Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
All product was distributed in the state of Florida.
Swai Fillets ( 7-9 oz.) packaged in a 15 lb. blue and white box with blue and white lettering.
1134 cases (A case is 1, 15 lb. box of fillets) Fillets per box vary
Nitrofuran (SCA) was found in the product during routine third party lab testing.
Product 39 consists of all product under  product code: JDI  and same usage:  Item no:	  32902605800	ION IMPLANTED FEM 22MM LO  32902604900	ION IMPLANTED FEM 26MM ME  32902603900	ION IMPLANTED FEM 26MM SH    For use in total or hemi hip arthroplasty
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013.  The affected products are sterile.
Product 31 consists of all product under  product code: KTT and same usage:  Item no:	  118113003	FREE-LOCK TUBE & SCP PLAT  118113502	FREE-LOCK TUBE & SCP PLAT  118113503	FREE-LOCK TUBE & SCP PLAT  118114002	FREE-LOCK TUBE & SCP PLAT  118114003	FREE-LOCK TUBE & SCP PLAT  118114502	FREE-LOCK TUBE & SCP PLAT  118114503	FREE-LOCK TUBE & SCP PLAT  118115002	FREE-LOCK TUBE & SCP PLAT  118115003	FREE-LOCK TUBE & SCP PLAT    Product Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 45 consists of all product under  product code: JWH and same usage:  Item no:	  511007020	MGII KNEE SLF-TAP BONE ST  511007025	MGII KNEE SLF-TAP BONE ST  511007030	MGII KNEE SLF-TAP BONE ST  511007035	MGII KNEE SLF-TAP BONE ST  511007040	MGII KNEE SLF-TAP BONE ST  511007045	MGII KNEE SLF-TAP BONE ST  for use in total knee arthroplasty
Product 67 consists of all product under product code: JDI and same usage:  Item no:	  785001100	VERSYS ADVOCATE CEMENTED  785001200	VERSYS ADVOCATE CEMENTED  785001220	VERSYS ADVOCATE CEMENTED  785001300	VERSYS ADVOCATE CEMENTED  785001320	VERSYS ADVOCATE CEMENTED  785001400	VERSYS ADVOCATE CEMENTED  785001420	VERSYS ADVOCATE CEMENTED  785001500	VERSYS ADVOCATE CEMENTED  785001520	VERSYS ADVOCATE CEMENTED  785001600	VERSYS ADVOCATE CEMENTED  785001620	VERSYS ADVOCATE CEMENTED  785001700	VERSYS ADVOCATE CEMENTED  785001305	VERSYS ADVOCATE V-LIGN CE  785001325	VERSYS ADVOCATE V-LIGN CE  785001405	VERSYS ADVOCATE V-LIGN CE  785001505	VERSYS ADVOCATE V-LIGN CE  785001525	VERSYS ADVOCATE V-LIGN CE    For use in total or hemi hip arthroplasty
Product 68 consists of all product under product code: JDI and same usage:  Item no:	  787101360	VERSYS CEM/REV/CALCAR 13X  787101361	VERSYS CEM/REV/CALCAR 13X  787101362	VERSYS CEM/REV/CALCAR 13X  787101363	VERSYS CEM/REV/CALCAR 13X  787101560	VERSYS CEM/REV/CALCAR 15X  787101561	VERSYS CEM/REV/CALCAR 15X  787101562	VERSYS CEM/REV/CALCAR 15X  787101563	VERSYS CEM/REV/CALCAR 15X  787101760	VERSYS CEM/REV/CALCAR 17X  787101761	VERSYS CEM/REV/CALCAR 17X  787101761	VERSYS CEM/REV/CALCAR 17X    For use in total or hemi hip arthroplasty
Product 64 consists of all product under product code: JDI and same usage:  Item no:	  902605101	UNIPOLAR ENDO FEM HEAD 51MM    For use in hemi hip arthroplasty
Product 44 consists of all product under  product code: HWC and same usage:  Item no:	  114607099	MAGMA-FX CANN SCREW 7.0MM  114604099	MAGNA FX CANN SCREW 7.0MM  114603000	MAGNA-FX CANN SCREW 7.0MM  114603500	MAGNA-FX CANN SCREW 7.0MM  114604000	MAGNA-FX CANN SCREW 7.0MM  114604032	MAGNA-FX CANN SCREW 7.0MM  114604500	MAGNA-FX CANN SCREW 7.0MM  114604532	MAGNA-FX CANN SCREW 7.0MM  114604599	MAGNA-FX CANN SCREW 7.0MM  114605000	MAGNA-FX CANN SCREW 7.0MM  114605032	MAGNA-FX CANN SCREW 7.0MM  114605099	MAGNA-FX CANN SCREW 7.0MM  114605500	MAGNA-FX CANN SCREW 7.0MM  114605532	MAGNA-FX CANN SCREW 7.0MM  114605599	MAGNA-FX CANN SCREW 7.0MM  114606000	MAGNA-FX CANN SCREW 7.0MM  114606032	MAGNA-FX CANN SCREW 7.0MM  114606099	MAGNA-FX CANN SCREW 7.0MM  114606500	MAGNA-FX CANN SCREW 7.0MM  114606532	MAGNA-FX CANN SCREW 7.0MM  114606599	MAGNA-FX CANN SCREW 7.0MM  114607000	MAGNA-FX CANN SCREW 7.0MM  114607032	MAGNA-FX CANN SCREW 7.0MM  114607500	MAGNA-FX CANN SCREW 7.0MM  114607532	MAGNA-FX CANN SCREW 7.0MM  114607599	MAGNA-FX CANN SCREW 7.0MM  114608000	MAGNA-FX CANN SCREW 7.0MM  114608032	MAGNA-FX CANN SCREW 7.0MM  114608099	MAGNA-FX CANN SCREW 7.0MM  114608500	MAGNA-FX CANN SCREW 7.0MM  114608532	MAGNA-FX CANN SCREW 7.0MM  114608599	MAGNA-FX CANN SCREW 7.0MM  114609000	MAGNA-FX CANN SCREW 7.0MM  114609032	MAGNA-FX CANN SCREW 7.0MM  114609099	MAGNA-FX CANN SCREW 7.0MM  114609500	MAGNA-FX CANN SCREW 7.0MM  114609532	MAGNA-FX CANN SCREW 7.0MM  114609599	MAGNA-FX CANN SCREW 7.0MM  114610000	MAGNA-FX CANN SCREW 7.0MM  114610032	MAGNA-FX CANN SCREW 7.0MM  114610099	MAGNA-FX CANN SCREW 7.0MM  114610500	MAGNA-FX CANN SCREW 7.0MM  114610532	MAGNA-FX CANN SCREW 7.0MM  114610599	MAGNA-FX CANN SCREW 7.0MM  114611000	MAGNA-FX CANN SCREW 7.0MM  114611032	MAGNA-FX CANN SCREW 7.0MM  114611099	MAGNA-FX CANN SCREW 7.0MM  114611500	MAGNA-FX CANN SCREW 7.0MM  114611532	MAGNA-FX CANN SCREW 7.0MM  114611599	MAGNA-FX CANN SCREW 7.0MM  114612000	MAGNA-FX CANN SCREW 7.0MM  114612032	MAGNA-FX CANN SCREW 7.0MM  114612500	MAGNA-FX CANN SCREW 7.0
Product 25 consists of all product under product code: LPH and same usage:  Item no:	  234703104	DISTAL MEDIAL FEMORAL CON  234703206	DISTAL MEDIAL FEMORAL CON  234703208	DISTAL MEDIAL FEMORAL CON  234800504	DISTAL POSTERIOR/LATERAL  234800506	DISTAL POSTERIOR/LATERAL  234800508	DISTAL POSTERIOR/LATERAL  234800510	DISTAL POSTERIOR/LATERAL  234800604	DISTAL POSTERIOR/LATERAL  234800606	DISTAL POSTERIOR/LATERAL  234800608	DISTAL POSTERIOR/LATERAL  234800610	DISTAL POSTERIOR/LATERAL  234800614	DISTAL POSTERIOR/LATERAL    For use in total hip arthroplasty
Product 17 consists of all product under   product code: LPH and same usage:  Item no:	  625004515	BONE SCREW 4.5X15 SELF-TA  625004520	BONE SCREW 4.5X20 SELF-TA  625004525	BONE SCREW 4.5X25 SELF-TA  625004530	BONE SCREW 4.5X30 SELF-TA  625004535	BONE SCREW 4.5X35 SELF-TA  625004540	BONE SCREW 4.5X40 SELF-TA  625004550	BONE SCREW 4.5X50 SELF-TA  625006515	BONE SCREW 6.5X15 SELF-TA  625006520	BONE SCREW 6.5X20 SELF-TA  625006525	BONE SCREW 6.5X25 SELF-TA  625006530	BONE SCREW 6.5X30 SELF-TA  625006535	BONE SCREW 6.5X35 SELF-TA  625006540	BONE SCREW 6.5X40 SELF-TA  625006550	BONE SCREW 6.5X50 SELF-TA  625006560	BONE SCREW 6.5X60 SELF-TA  625006570	BONE SCREW 6.5X70 SELF-TA    Product Usage:  For use in total or hemi hip arthroplasty
Product 35 consists of all product under   product code: JWH and same usage:  Item no:	  522007300	I/B II KNEE FLUTED ROD, 1    for use in total knee arthroplasty
Product 55 consists of all product under product code: HSB and same usage:  Item no:	  225900132	ONE-PIECE LAG SCREW 11MM  225900135	ONE-PIECE LAG SCREW 11MM  225900137	ONE-PIECE LAG SCREW 11MM  225900140	ONE-PIECE LAG SCREW 11MM  225900142	ONE-PIECE LAG SCREW 11MM  225900145	ONE-PIECE LAG SCREW 11MM  225900152	ONE-PIECE LAG SCREW 11MM  Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 28 consists of all product under product code: JDI and same usage:  Item no:	  32902605000	FEMORAL HD 28MM MEDIUM  32902604000	FEMORAL HD 28MM SHORT  32902604035	FEMORAL HD 28MM SHT+ 3.5M    For use in total or hemi hip arthroplasty
Product 46 consists of all product under  product code: HWC and same usage:  Item no:	  114204012	MINI MAGNA-FX CANN SCREW  114204016	MINI MAGNA-FX CANN SCREW  114204020	MINI MAGNA-FX CANN SCREW  114204024	MINI MAGNA-FX CANN SCREW  114204028	MINI MAGNA-FX CANN SCREW  114204032	MINI MAGNA-FX CANN SCREW  114204036	MINI MAGNA-FX CANN SCREW  114204040	MINI MAGNA-FX CANN SCREW  114204044	MINI MAGNA-FX CANN SCREW  114204048	MINI MAGNA-FX CANN SCREW  114204055	MINI MAGNA-FX CANN SCREW  114204065	MINI MAGNA-FX CANN SCREW  114204124	MINI MAGNA-FX CANN SCREW  114204126	MINI MAGNA-FX CANN SCREW  114204128	MINI MAGNA-FX CANN SCREW  114204130	MINI MAGNA-FX CANN SCREW  114204132	MINI MAGNA-FX CANN SCREW  114204134	MINI MAGNA-FX CANN SCREW  114204136	MINI MAGNA-FX CANN SCREW  114204138	MINI MAGNA-FX CANN SCREW  114204140	MINI MAGNA-FX CANN SCREW  114204142	MINI MAGNA-FX CANN SCREW  114204144	MINI MAGNA-FX CANN SCREW  114204146	MINI MAGNA-FX CANN SCREW  114204148	MINI MAGNA-FX CANN SCREW  114204150	MINI MAGNA-FX CANN SCREW  114204155	MINI MAGNA-FX CANN SCREW  114204160	MINI MAGNA-FX CANN SCREW  114204165	MINI MAGNA-FX CANN SCREW  114204170	MINI MAGNA-FX CANN SCREW  114205012	MINI MAGNA-FX CANN SCREW  114205016	MINI MAGNA-FX CANN SCREW  114205020	MINI MAGNA-FX CANN SCREW  114205024	MINI MAGNA-FX CANN SCREW  114205028	MINI MAGNA-FX CANN SCREW  114205032	MINI MAGNA-FX CANN SCREW  114205036	MINI MAGNA-FX CANN SCREW  114205040	MINI MAGNA-FX CANN SCREW  114205044	MINI MAGNA-FX CANN SCREW  114205048	MINI MAGNA-FX CANN SCREW  114205055	MINI MAGNA-FX CANN SCREW  114205065	MINI MAGNA-FX CANN SCREW  114205124	MINI MAGNA-FX CANN SCREW  114205126	MINI MAGNA-FX CANN SCREW  114205128	MINI MAGNA-FX CANN SCREW  114205130	MINI MAGNA-FX CANN SCREW  114205132	MINI MAGNA-FX CANN SCREW  114205134	MINI MAGNA-FX CANN SCREW  114205136	MINI MAGNA-FX CANN SCREW  114205138	MINI MAGNA-FX CANN SCREW  114205140	MINI MAGNA-FX CANN SCREW  114205142	MINI MAGNA-FX CANN SCREW  114205144	MINI MAGNA-FX CANN SCREW  114205146	MINI MAGNA-FX CANN SCREW  114205148	MIN
Product 22 consists of all product under   product code: JDI and same usage:  Item no:	  811400218	CPT 12/14 COCR REVISION S  811400318	CPT 12/14 COCR REVISION S  811400420	CPT 12/14 COCR REVISION S  811400423	CPT 12/14 COCR REVISION S  811400426	CPT 12/14 COCR REVISION S  811400010	CPT 12/14 COCR SIZE 0 EXT  811400000	CPT 12/14 COCR SIZE 0 STD  811400110	CPT 12/14 COCR SIZE 1 EXT  811400100	CPT 12/14 COCR SIZE 1 STD  811400210	CPT 12/14 COCR SIZE 2 EXT  811400200	CPT 12/14 COCR SIZE 2 STD  811400230	CPT 12/14 COCR SIZE 2 XEX  811400310	CPT 12/14 COCR SIZE 3 EXT  811400300	CPT 12/14 COCR SIZE 3 STD  811400330	CPT 12/14 COCR SIZE 3 XEX  811400410	CPT 12/14 COCR SIZE 4 EXT  811400400	CPT 12/14 COCR SIZE 4 STD  811400430	CPT 12/14 COCR SIZE 4 XEX  811400510	CPT 12/14 COCR SIZE 5 EXT  811400500	CPT 12/14 COCR SIZE 5 STD  811400530	CPT 12/14 COCR SIZE 5 XEX    For use in total or hemi hip arthroplasty
Product 69 consists of all product under product code: JDI and same usage:  Item no:	  785301701	VERSYS CEMENTED FEM STEM  785301521	VERSYS CEMENTED FEM STEM 15X140MM X-OFF  785301601	VERSYS CEMENTED FEM STEM 16X145MM    For use in total or hemi hip arthroplasty
Product 61 consists of all product under product code: JWH and same usage:  Item no:	  598003712	STD PRECOAT TIBIA PLATE S    for use in total knee arthroplasty
Product 47 consists of all product under  product code: LPH and same usage:  Item no:	  611004022	MODULAR CUP 10 DEGREE LIN  611004428	MODULAR CUP 10 DEGREE LIN  611004628	MODULAR CUP 10 DEGREE LIN  611004828	MODULAR CUP 10 DEGREE LIN  611004832	MODULAR CUP 10 DEGREE LIN  611005028	MODULAR CUP 10 DEGREE LIN  611005032	MODULAR CUP 10 DEGREE LIN  611005628	MODULAR CUP 10 DEGREE LIN  611005632	MODULAR CUP 10 DEGREE LIN  611005828	MODULAR CUP 10 DEGREE LIN  611005832	MODULAR CUP 10 DEGREE LIN  611006028	MODULAR CUP 10 DEGREE LIN  611006032	MODULAR CUP 10 DEGREE LIN  611006228	MODULAR CUP 10 DEGREE LIN  611006232	MODULAR CUP 10 DEGREE LIN  611006428	MODULAR CUP 10 DEGREE LIN  611006432	MODULAR CUP 10 DEGREE LIN  611006628	MODULAR CUP 10 DEGREE LIN  611006832	MODULAR CUP 10 DEGREE LIN  611007028	MODULAR CUP 10 DEGREE LIN  612004626	MODULAR CUP 20 DEGREE LIN  612004628	MODULAR CUP 20 DEGREE LIN  612004828	MODULAR CUP 20 DEGREE LIN  612004832	MODULAR CUP 20 DEGREE LIN  612005028	MODULAR CUP 20 DEGREE LIN  612005032	MODULAR CUP 20 DEGREE LIN  612005628	MODULAR CUP 20 DEGREE LIN  612005828	MODULAR CUP 20 DEGREE LIN  612005832	MODULAR CUP 20 DEGREE LIN  612006028	MODULAR CUP 20 DEGREE LIN  612006032	MODULAR CUP 20 DEGREE LIN  610504428	MODULAR CUP NEUTRAL LINER  610504832	MODULAR CUP NEUTRAL LINER  610505028	MODULAR CUP NEUTRAL LINER  610505032	MODULAR CUP NEUTRAL LINER  610505632	MODULAR CUP NEUTRAL LINER  610505832	MODULAR CUP NEUTRAL LINER  610506032	MODULAR CUP NEUTRAL LINER  610506232	MODULAR CUP NEUTRAL LINER    For use in total hip arthroplasty
Product 48 consists of all product under  product code: JWH and same usage:  Item no:	  597206526	NEXGEN ALL-POLY PATELLA,    for use in total knee arthroplasty
Product 65 consists of all product under product code: KTT and same usage:  Item no:	  119413594	VERSA-FX II KEYLESS SHORT  119413595	VERSA-FX II KEYLESS SHORT  119413596	VERSA-FX II KEYLESS SHORT  119413004	VERSA-FX II KEYLESS TUBE  119413005	VERSA-FX II KEYLESS TUBE  119413006	VERSA-FX II KEYLESS TUBE  119413008	VERSA-FX II KEYLESS TUBE  119413504	VERSA-FX II KEYLESS TUBE  119413505	VERSA-FX II KEYLESS TUBE  119413506	VERSA-FX II KEYLESS TUBE  119413508	VERSA-FX II KEYLESS TUBE  119414004	VERSA-FX II KEYLESS TUBE  119414005	VERSA-FX II KEYLESS TUBE  119414006	VERSA-FX II KEYLESS TUBE  119414008	VERSA-FX II KEYLESS TUBE  119414504	VERSA-FX II KEYLESS TUBE  119414506	VERSA-FX II KEYLESS TUBE  119414508	VERSA-FX II KEYLESS TUBE  119415004	VERSA-FX II KEYLESS TUBE  119415005	VERSA-FX II KEYLESS TUBE  119415006	VERSA-FX II KEYLESS TUBE  119415008	VERSA-FX II KEYLESS TUBE  119313094	VERSA-FX II SHORT TUBE PL  119313095	VERSA-FX II SHORT TUBE PL  119313096	VERSA-FX II SHORT TUBE PL  119313594	VERSA-FX II SHORT TUBE PL  119313595	VERSA-FX II SHORT TUBE PL  119313596	VERSA-FX II SHORT TUBE PL  119314094	VERSA-FX II SHORT TUBE PL  119314594	VERSA-FX II SHORT TUBE PL  119314595	VERSA-FX II SHORT TUBE PL  119315094	VERSA-FX II SHORT TUBE PL  119315095	VERSA-FX II SHORT TUBE PL  119313002	VERSA-FX II STD TUBE PLAT  119313003	VERSA-FX II STD TUBE PLAT  119313004	VERSA-FX II STD TUBE PLAT  119313005	VERSA-FX II STD TUBE PLAT  119313006	VERSA-FX II STD TUBE PLAT  119313008	VERSA-FX II STD TUBE PLAT  119313010	VERSA-FX II STD TUBE PLAT  119313012	VERSA-FX II STD TUBE PLAT  119313502	VERSA-FX II STD TUBE PLAT  119313503	VERSA-FX II STD TUBE PLAT  119313504	VERSA-FX II STD TUBE PLAT  119313505	VERSA-FX II STD TUBE PLAT  119313506	VERSA-FX II STD TUBE PLAT  119313508	VERSA-FX II STD TUBE PLAT  119313510	VERSA-FX II STD TUBE PLAT  119313512	VERSA-FX II STD TUBE PLAT  119314002	VERSA-FX II STD TUBE PLAT  119314003	VERSA-FX II STD TUBE PLAT  119314004	VERSA-FX II STD TUBE PLAT  119314005	VERSA-FX II STD TUBE PLAT  119314006	VERSA-
Product 66 consists of all product under product code: JDI and same usage:  Item no:	  785001100	VERSYS ADVOCATE CEMENTED  785001200	VERSYS ADVOCATE CEMENTED  785001220	VERSYS ADVOCATE CEMENTED  785001300	VERSYS ADVOCATE CEMENTED  785001320	VERSYS ADVOCATE CEMENTED  785001400	VERSYS ADVOCATE CEMENTED  785001420	VERSYS ADVOCATE CEMENTED  785001500	VERSYS ADVOCATE CEMENTED  785001520	VERSYS ADVOCATE CEMENTED  785001600	VERSYS ADVOCATE CEMENTED  785001620	VERSYS ADVOCATE CEMENTED  785001700	VERSYS ADVOCATE CEMENTED  785001305	VERSYS ADVOCATE V-LIGN CE  785001325	VERSYS ADVOCATE V-LIGN CE  785001405	VERSYS ADVOCATE V-LIGN CE  785001505	VERSYS ADVOCATE V-LIGN CE  785001525	VERSYS ADVOCATE V-LIGN CE    For use in total or hemi hip arthroplasty
Product 21 consists of all product under  product code: JDI and same usage:  Item no:	  811400218	CPT 12/14 COCR REVISION S  811400318	CPT 12/14 COCR REVISION S  811400420	CPT 12/14 COCR REVISION S  811400423	CPT 12/14 COCR REVISION S  811400426	CPT 12/14 COCR REVISION S  811400010	CPT 12/14 COCR SIZE 0 EXT  811400000	CPT 12/14 COCR SIZE 0 STD  811400110	CPT 12/14 COCR SIZE 1 EXT  811400100	CPT 12/14 COCR SIZE 1 STD  811400210	CPT 12/14 COCR SIZE 2 EXT  811400200	CPT 12/14 COCR SIZE 2 STD  811400230	CPT 12/14 COCR SIZE 2 XEX  811400310	CPT 12/14 COCR SIZE 3 EXT  811400300	CPT 12/14 COCR SIZE 3 STD  811400330	CPT 12/14 COCR SIZE 3 XEX  811400410	CPT 12/14 COCR SIZE 4 EXT  811400400	CPT 12/14 COCR SIZE 4 STD  811400430	CPT 12/14 COCR SIZE 4 XEX  811400510	CPT 12/14 COCR SIZE 5 EXT  811400500	CPT 12/14 COCR SIZE 5 STD  811400530	CPT 12/14 COCR SIZE 5 XEX    Product Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 18 consists of all product under  product code: HWC and same usage:  Item no:	  47248001441	CANC SCR 4.0MM X 14MM FUL  47248001641	CANC SCR 4.0MM X 16MM FUL  47248001840	CANC SCR 4.0MM X 18MM  47248001841	CANC SCR 4.0MM X 18MM FUL  47248002041	CANC SCR 4.0MM X 20MM FUL  47248002441	CANC SCR 4.0MM X 24MM FUL  47248003641	CANC SCR 4.0MM X 36MM FUL    Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 58 consists of all product under product code: HRS and same usage:  Item no:	  234800904	PROXIMAL DORSAL ULNA PLT  234800906	PROXIMAL DORSAL ULNA PLT  234800908	PROXIMAL DORSAL ULNA PLT  234800910	PROXIMAL DORSAL ULNA PLT  234801004	PROXIMAL DORSAL ULNA PLT  234801006	PROXIMAL DORSAL ULNA PLT  234801008	PROXIMAL DORSAL ULNA PLT  234801010	PROXIMAL DORSAL ULNA PLT 10H LT  234701304	PROXIMAL MEDIAL TIBIAL 4.  234701306	PROXIMAL MEDIAL TIBIAL 4.  234701308	PROXIMAL MEDIAL TIBIAL 4.  234701404	PROXIMAL MEDIAL TIBIAL 4.  234701406	PROXIMAL MEDIAL TIBIAL 4.  234701408	PROXIMAL MEDIAL TIBIAL 4.    Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 30 consists of all product under  product code: KTT and same usage:  Item no:	  118100527	FREE-LOCK LAG SCREW, 12.7  118100535	FREE-LOCK LAG SCREW, 12.7  118100540	FREE-LOCK LAG SCREW, 12.7  118100542	FREE-LOCK LAG SCREW, 12.7  118101022	FREE-LOCK LAG SCREW, 12.7  118101025	FREE-LOCK LAG SCREW, 12.7  118101027	FREE-LOCK LAG SCREW, 12.7  118101030	FREE-LOCK LAG SCREW, 12.7  118101032	FREE-LOCK LAG SCREW, 12.7  118101035	FREE-LOCK LAG SCREW, 12.7  118101037	FREE-LOCK LAG SCREW, 12.7  118101040	FREE-LOCK LAG SCREW, 12.7  118101042	FREE-LOCK LAG SCREW, 12.7  118101045	FREE-LOCK LAG SCREW, 12.7  118101047	FREE-LOCK LAG SCREW, 12.7  118101052	FREE-LOCK LAG SCREW, 12.7  118101055	FREE-LOCK LAG SCREW, 12.7  118101057	FREE-LOCK LAG SCREW, 12.7  118101522	FREE-LOCK LAG SCREW, 15.8  118101525	FREE-LOCK LAG SCREW, 15.8  118101527	FREE-LOCK LAG SCREW, 15.8  118101530	FREE-LOCK LAG SCREW, 15.8  118101532	FREE-LOCK LAG SCREW, 15.8  118101547	FREE-LOCK LAG SCREW, 15.8  118109010	FREE-LOCK SUPRACOND TUBE/  118109510	FREE-LOCK SUPRACOND TUBE/  118113005	FREE-LOCK TUBE & SCP PLAT  118113006	FREE-LOCK TUBE & SCP PLAT  118113010	FREE-LOCK TUBE & SCP PLAT  118113504	FREE-LOCK TUBE & SCP PLAT  118113505	FREE-LOCK TUBE & SCP PLAT  118113506	FREE-LOCK TUBE & SCP PLAT  118113508	FREE-LOCK TUBE & SCP PLAT  118113510	FREE-LOCK TUBE & SCP PLAT  118113594	FREE-LOCK TUBE & SCP PLAT  118114005	FREE-LOCK TUBE & SCP PLAT  118114006	FREE-LOCK TUBE & SCP PLAT  118114008	FREE-LOCK TUBE & SCP PLAT  118114010	FREE-LOCK TUBE & SCP PLAT  118114012	FREE-LOCK TUBE & SCP PLAT  118114004	FREE-LOCK TUBE & SCP PLAT  118114008	FREE-LOCK TUBE & SCP PLAT  118114010	FREE-LOCK TUBE & SCP PLAT  118114012	FREE-LOCK TUBE & SCP PLAT  118114504	FREE-LOCK TUBE & SCP PLAT  118114505	FREE-LOCK TUBE & SCP PLAT  118114506	FREE-LOCK TUBE & SCP PLAT  118114508	FREE-LOCK TUBE & SCP PLAT  118114512	FREE-LOCK TUBE & SCP PLAT  118114594	FREE-LOCK TUBE & SCP PLAT  118114508	FREE-LOCK TUBE & SCP PLAT  118114512	FREE-LOCK TUBE & SCP PLAT  118114594	FREE-LOCK TUBE & SCP PL
Product 60 consists of all product under product code: HSB and same usage:  Item no:	  225207055	RECON SCREW LG 5.5MM DIA  225207555	RECON SCREW LG 5.5MM DIA  225208055	RECON SCREW LG 5.5MM DIA  225208555	RECON SCREW LG 5.5MM DIA  225209055	RECON SCREW LG 5.5MM DIA  225209555	RECON SCREW LG 5.5MM DIA  225210055	RECON SCREW LG 5.5MM DIA  225210555	RECON SCREW LG 5.5MM DIA  225211555	RECON SCREW LG 5.5MM DIA  225212055	RECON SCREW LG 5.5MM DIA  225213055	RECON SCREW LG 5.5MM DIA    Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 36 consists of all product under  product code: HSB and same usage:  Item no:	  225302745	INTERLOCKING IM SCREW 4.5  225303045	INTERLOCKING IM SCREW 4.5  225303245	INTERLOCKING IM SCREW 4.5  225303545	INTERLOCKING IM SCREW 4.5  225303745	INTERLOCKING IM SCREW 4.5  225304045	INTERLOCKING IM SCREW 4.5  225304245	INTERLOCKING IM SCREW 4.5  225304545	INTERLOCKING IM SCREW 4.5  225305045	INTERLOCKING IM SCREW 4.5  225305245	INTERLOCKING IM SCREW 4.5  225305545	INTERLOCKING IM SCREW 4.5  225305745	INTERLOCKING IM SCREW 4.5  225306045	INTERLOCKING IM SCREW 4.5  225306545	INTERLOCKING IM SCREW 4.5  225307045	INTERLOCKING IM SCREW 4.5    Product Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 15 consists of all product code JDI  , and same usage:  Item no:	  805002802	ASTEL FEM HEAD +0X28MM DI  805002805	ASTEL FEM HEAD +10.5X28MM  805002803	ASTEL FEM HEAD +3.5X28MM  805002804	ASTEL FEM HEAD +7X28MM DI  805002801	ASTEL FEM HEAD -3.5X28MM    Usage:  For use in total or hemi hip arthroplasty
Product 40 consists of all product under  product code: HSB and same usage:  Item no:	  225706565	ITST ANTI-ROTATION SCREW  225707065	ITST ANTI-ROTATION SCREW  225708065	ITST ANTI-ROTATION SCREW  225708565	ITST ANTI-ROTATION SCREW  225709065	ITST ANTI-ROTATION SCREW    Product Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 42 consists of all product under  product code: HSB and same usage:  Item no:	  225224010	M/DN FEM IM NAIL 10MM DIA  225228010	M/DN FEM IM NAIL 10MM DIA  225230010	M/DN FEM IM NAIL 10MM DIA  225232010	M/DN FEM IM NAIL 10MM DIA  225234010	M/DN FEM IM NAIL 10MM DIA  225236010	M/DN FEM IM NAIL 10MM DIA  225238010	M/DN FEM IM NAIL 10MM DIA  225240010	M/DN FEM IM NAIL 10MM DIA  225242010	M/DN FEM IM NAIL 10MM DIA  225244010	M/DN FEM IM NAIL 10MM DIA  225246010	M/DN FEM IM NAIL 10MM DIA  225228011	M/DN FEM IM NAIL 11MM DIA  225230011	M/DN FEM IM NAIL 11MM DIA  225232011	M/DN FEM IM NAIL 11MM DIA  225234011	M/DN FEM IM NAIL 11MM DIA  225236011	M/DN FEM IM NAIL 11MM DIA  225238011	M/DN FEM IM NAIL 11MM DIA  225240011	M/DN FEM IM NAIL 11MM DIA  225242011	M/DN FEM IM NAIL 11MM DIA  225244011	M/DN FEM IM NAIL 11MM DIA  225246011	M/DN FEM IM NAIL 11MM DIA  225224012	M/DN FEM IM NAIL 12MM DIA  225232012	M/DN FEM IM NAIL 12MM DIA  225234012	M/DN FEM IM NAIL 12MM DIA  225236012	M/DN FEM IM NAIL 12MM DIA  225238012	M/DN FEM IM NAIL 12MM DIA  225240012	M/DN FEM IM NAIL 12MM DIA  225242012	M/DN FEM IM NAIL 12MM DIA  225244012	M/DN FEM IM NAIL 12MM DIA  225246012	M/DN FEM IM NAIL 12MM DIA  225228013	M/DN FEM IM NAIL 13MM DIA  225230013	M/DN FEM IM NAIL 13MM DIA  225232013	M/DN FEM IM NAIL 13MM DIA  225234013	M/DN FEM IM NAIL 13MM DIA  225236013	M/DN FEM IM NAIL 13MM DIA  225238013	M/DN FEM IM NAIL 13MM DIA  225240013	M/DN FEM IM NAIL 13MM DIA  225242013	M/DN FEM IM NAIL 13MM DIA  225244013	M/DN FEM IM NAIL 13MM DIA  225246013	M/DN FEM IM NAIL 13MM DIA  225236014	M/DN FEM IM NAIL 14MM DIA  225238014	M/DN FEM IM NAIL 14MM DIA  225240014	M/DN FEM IM NAIL 14MM DIA  225242014	M/DN FEM IM NAIL 14MM DIA  225244014	M/DN FEM IM NAIL 14MM DIA  225246014	M/DN FEM IM NAIL 14MM DIA  225234015	M/DN FEM IM NAIL 15MM DIA  225240015	M/DN FEM IM NAIL 15MM DIA  225242015	M/DN FEM IM NAIL 15MM DIA  225244015	M/DN FEM IM NAIL 15MM DIA  225242016	M/DN FEM IM NAIL 16MM DIA  225230008	M/DN FEM IM NAIL 8MM DIA  225232008	M/DN FEM IM NAIL 8MM DIA
Product 32 consists of all product under  product code: HWC and same usage:  Item no:	  47115401200	HERBERT BONE SCREW, 3.0MM  47115401400	HERBERT BONE SCREW, 3.0MM  47115401600	HERBERT BONE SCREW, 3.0MM  47115401800	HERBERT BONE SCREW, 3.0MM  47115402000	HERBERT BONE SCREW, 3.0MM  47115402200	HERBERT BONE SCREW, 3.0MM  47115402400	HERBERT BONE SCREW, 3.0MM  47115402600	HERBERT BONE SCREW, 3.0MM  47115402800	HERBERT BONE SCREW, 3.0MM  47115403000	HERBERT BONE SCREW, 3.0MM  47115502505	HERBERT CANNULATED BONE S  47115503005	HERBERT CANNULATED BONE S  47115503505	HERBERT CANNULATED BONE S  47115504005	HERBERT CANNULATED BONE S  47115504007	HERBERT CANNULATED BONE S  47115504505	HERBERT CANNULATED BONE S  47115504507	HERBERT CANNULATED BONE S  47115505005	HERBERT CANNULATED BONE S  47115505007	HERBERT CANNULATED BONE S  47115505505	HERBERT CANNULATED BONE S  47115505507	HERBERT CANNULATED BONE S  47115506005	HERBERT CANNULATED BONE S  47115506007	HERBERT CANNULATED BONE S  47115506505	HERBERT CANNULATED BONE S  47115506507	HERBERT CANNULATED BONE S  47115507005	HERBERT CANNULATED BONE S  47115507007	HERBERT CANNULATED BONE S  47115507505	HERBERT CANNULATED BONE S  47115507507	HERBERT CANNULATED BONE S  47115508005	HERBERT CANNULATED BONE S  47115508007	HERBERT CANNULATED BONE S  47115508505	HERBERT CANNULATED BONE S  47115508507	HERBERT CANNULATED BONE S  47115509005	HERBERT CANNULATED BONE S  47115509007	HERBERT CANNULATED BONE S  47115509505	HERBERT CANNULATED BONE S  47115509507	HERBERT CANNULATED BONE S  47115510005	HERBERT CANNULATED BONE S  47115510007	HERBERT CANNULATED BONE S  115001000	HERBERT MINI BONE SCREW 2  115001200	HERBERT MINI BONE SCREW 2  115001400	HERBERT MINI BONE SCREW 2  115001600	HERBERT MINI BONE SCREW 2  115001800	HERBERT MINI BONE SCREW 2  115002000	HERBERT MINI BONE SCREW 2  115002200	HERBERT MINI BONE SCREW 2  115002400	HERBERT MINI BONE SCREW 2  115201200	HERBERT/WHIPPLE CANN BONE  115201400	HERBERT/WHIPPLE CANN BONE  115201600	HERBERT/WHIPPLE CANN BONE  115201800	HERBERT/WHIPPLE CAN
Product 43 consists of all product under  product code: HSB and same usage:  Item no:	  224001016	M/DN R-F IM NAIL 10MM DIA  224001018	M/DN R-F IM NAIL 10MM DIA  224001020	M/DN R-F IM NAIL 10MM DIA  224001022	M/DN R-F IM NAIL 10MM DIA  224001024	M/DN R-F IM NAIL 10MM DIA  224001026	M/DN R-F IM NAIL 10MM DIA  224001028	M/DN R-F IM NAIL 10MM DIA  224001030	M/DN R-F IM NAIL 10MM DIA  224001032	M/DN R-F IM NAIL 10MM DIA  224001034	M/DN R-F IM NAIL 10MM DIA  224001036	M/DN R-F IM NAIL 10MM DIA  224001038	M/DN R-F IM NAIL 10MM DIA  224001040	M/DN R-F IM NAIL 10MM DIA  224001042	M/DN R-F IM NAIL 10MM DIA  224001114	M/DN R-F IM NAIL 11MM DIA  224001116	M/DN R-F IM NAIL 11MM DIA  224001118	M/DN R-F IM NAIL 11MM DIA  224001120	M/DN R-F IM NAIL 11MM DIA  224001122	M/DN R-F IM NAIL 11MM DIA  224001124	M/DN R-F IM NAIL 11MM DIA  224001126	M/DN R-F IM NAIL 11MM DIA  224001128	M/DN R-F IM NAIL 11MM DIA  224001130	M/DN R-F IM NAIL 11MM DIA  224001132	M/DN R-F IM NAIL 11MM DIA  224001134	M/DN R-F IM NAIL 11MM DIA  224001136	M/DN R-F IM NAIL 11MM DIA  224001138	M/DN R-F IM NAIL 11MM DIA  224001140	M/DN R-F IM NAIL 11MM DIA  224001142	M/DN R-F IM NAIL 11MM DIA  224001144	M/DN R-F IM NAIL 11MM DIA  224001146	M/DN R-F IM NAIL 11MM DIA  224001218	M/DN R-F IM NAIL 12MM DIA  224001220	M/DN R-F IM NAIL 12MM DIA  224001224	M/DN R-F IM NAIL 12MM DIA  224001226	M/DN R-F IM NAIL 12MM DIA  224001228	M/DN R-F IM NAIL 12MM DIA  224001230	M/DN R-F IM NAIL 12MM DIA  224001232	M/DN R-F IM NAIL 12MM DIA  224001234	M/DN R-F IM NAIL 12MM DIA  224001236	M/DN R-F IM NAIL 12MM DIA  224001238	M/DN R-F IM NAIL 12MM DIA  224001240	M/DN R-F IM NAIL 12MM DIA  224001242	M/DN R-F IM NAIL 12MM DIA  224001244	M/DN R-F IM NAIL 12MM DIA  224001248	M/DN R-F IM NAIL 12MM DIA  224001318	M/DN R-F IM NAIL 13MM DIA  224001324	M/DN R-F IM NAIL 13MM DIA  224001326	M/DN R-F IM NAIL 13MM DIA  224001328	M/DN R-F IM NAIL 13MM DIA  224001330	M/DN R-F IM NAIL 13MM DIA  224001332	M/DN R-F IM NAIL 13MM DIA  224001334	M/DN R-F IM NAIL 13MM DIA  224001336	M/DN R-F IM NAIL 13MM D
Product 49 consists of all product under  product code: JWH and same usage:  Item no:	  597206529	NEXGEN ALL-POLY PATELLA,  597206532	NEXGEN ALL-POLY PATELLA,  597206535	NEXGEN ALL-POLY PATELLA,  597206538	NEXGEN ALL-POLY PATELLA,  597206541	NEXGEN ALL-POLY PATELLA,  598801713	NEXGEN CEMENTED STEM EXT  598801813	NEXGEN CEMENTED STEM EXT  598801913	NEXGEN CEMENTED STEM EXT  598801610	NEXGEN FLUTED STEM EXT, 1  598801611	NEXGEN FLUTED STEM EXT, 1  598801612	NEXGEN FLUTED STEM EXT, 1  598801613	NEXGEN FLUTED STEM EXT, 1  598801614	NEXGEN FLUTED STEM EXT, 1  598801615	NEXGEN FLUTED STEM EXT, 1  598801616	NEXGEN FLUTED STEM EXT, 1  598801618	NEXGEN FLUTED STEM EXT, 1  598801619	NEXGEN FLUTED STEM EXT, 1  598801620	NEXGEN FLUTED STEM EXT, 2  598801622	NEXGEN FLUTED STEM EXT, 2  598801624	NEXGEN FLUTED STEM EXT, 2  597206126	NEXGEN MICRO ALL-POLY PAT  597206129	NEXGEN MICRO ALL-POLY PAT  597206132	NEXGEN MICRO ALL-POLY PAT  597206135	NEXGEN MICRO ALL-POLY PAT    for use in total knee arthroplasty
Product 19 consists of all product code: JDI and same usage:  Item no:	  765301101	CEM FEM ST 11X120 NOCOAT  765301201	CEM FEM ST 12X125 NOCOAT  765301301	CEM FEM ST 13X130 NOCOAT  765301401	CEM FEM ST 14X135 NOCOAT  765301501	CEM FEM ST 15X140 NOCOAT  765301601	CEM FEM ST 16X145 NOCOAT  763301300	CEM FEM ST FX 13 X 130  763301600	CEM FEM ST FX 16 X 145    For use in total or hemi hip arthroplasty
Product 10consists of all product under product code HWC, and same usage:  Item no:	  47484502601	4.5 X 26 CORT SCREW SELF  	  	  Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 33 consists of all product under  product code: JDI and same usage:  Item no:	  662406515	HGP II ACETABULAR CUP BON  662406520	HGP II ACETABULAR CUP BON  662406525	HGP II ACETABULAR CUP BON  662406530	HGP II ACETABULAR CUP BON  662406535	HGP II ACETABULAR CUP BON  662406540	HGP II ACETABULAR CUP BON  662406550	HGP II ACETABULAR CUP BON  662406560	HGP II ACETABULAR CUP BON    For use in total hip arthroplasty
Product 29 consists of all product under  product code: LPHand same usage:  Item no:	  32902603800	FEMORAL HEAD +0.5 X 22 MM  32902604810	FEMORAL HEAD +3.5 X 22 MM  32902604845	FEMORAL HEAD +7.0 X 22 MM    For use in total or hemi hip arthroplasty
Product 27 consists of all product under  product code: HSB and same usage:  Item no:	  234703104	DISTAL MEDIAL FEMORAL CON  234703206	DISTAL MEDIAL FEMORAL CON  234703208	DISTAL MEDIAL FEMORAL CON  234800504	DISTAL POSTERIOR/LATERAL  234800506	DISTAL POSTERIOR/LATERAL  234800508	DISTAL POSTERIOR/LATERAL  234800510	DISTAL POSTERIOR/LATERAL  234800604	DISTAL POSTERIOR/LATERAL  234800606	DISTAL POSTERIOR/LATERAL  234800608	DISTAL POSTERIOR/LATERAL  234800610	DISTAL POSTERIOR/LATERAL  234800614	DISTAL POSTERIOR/LATERAL    Product Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 52 consists of product code: HWC and same usage:  Item no:	  525004530	NEXGEN OSTEOTOMY CORT BON  525004540	NEXGEN OSTEOTOMY CORT BON  525006545	NEXGEN OSTEOTOMY CORT BON  525006560	NEXGEN OSTEOTOMY CORT BON  525006565	NEXGEN OSTEOTOMY CORT BON    for use in total knee arthroplasty
Product 63 consists of all product under product code: LPH and same usage:  Item no:	  620004020	TRILOGY ACET SHELL 40MM O  620004220	TRILOGY ACET SHELL 42MM O  620004420	TRILOGY ACET SHELL 44MM O  620004620	TRILOGY ACET SHELL 46MM O  620004621	TRILOGY ACET SHELL 46MM O  620004820	TRILOGY ACET SHELL 48MM O  620004822	TRILOGY ACET SHELL 48MM O  620004823	TRILOGY ACET SHELL 48MM O  620005020	TRILOGY ACET SHELL 50MM O  620005021	TRILOGY ACET SHELL 50MM O  620005022	TRILOGY ACET SHELL 50MM O  620005220	TRILOGY ACET SHELL 52MM O  620005221	TRILOGY ACET SHELL 52MM O  620005222	TRILOGY ACET SHELL 52MM O  620005223	TRILOGY ACET SHELL 52MM O  620005420	TRILOGY ACET SHELL 54MM O  620005421	TRILOGY ACET SHELL 54MM O  620005422	TRILOGY ACET SHELL 54MM O  620005423	TRILOGY ACET SHELL 54MM O  620005620	TRILOGY ACET SHELL 56MM O  620005621	TRILOGY ACET SHELL 56MM O  620005622	TRILOGY ACET SHELL 56MM O  620005623	TRILOGY ACET SHELL 56MM O  620005820	TRILOGY ACET SHELL 58MM O  620005821	TRILOGY ACET SHELL 58MM O  620005822	TRILOGY ACET SHELL 58MM O  620005823	TRILOGY ACET SHELL 58MM O  620006020	TRILOGY ACET SHELL 60MM O  620006022	TRILOGY ACET SHELL 60MM O  620006023	TRILOGY ACET SHELL 60MM O  620006021	TRILOGY ACET SHELL 60MM OD SOLID  620006220	TRILOGY ACET SHELL 62MM O  620006221	TRILOGY ACET SHELL 62MM O  620006222	TRILOGY ACET SHELL 62MM O  620006420	TRILOGY ACET SHELL 64MM O  620006422	TRILOGY ACET SHELL 64MM O  620006620	TRILOGY ACET SHELL 66MM O  For use in total hip arthroplasty
Product 12 consists of all product under product code JDI  , and same usage:  Item no:	  902602935	6 DEGREE COCR FEM HEAD 28  902602835	6 DEGREE COCR FEM HEAD 28  902603235	6 DEGREE COCR FEM HEAD 32  902603335	6 DEGREE COCR FEM HEAD 32  902603600	6 DEGREE COCR FEM HEAD 36  902603610	6 DEGREE COCR FEM HEAD 36  902603614	6 DEGREE COCR FEM HEAD 36    Product Usage:  For use in total or hemi hip arthroplasty
Product 6 consists of all products under  product code HWC, and same usage:  Item no:	  47493501001	3.5 X 10 CORT SCREW SELFT  47493501801	3.5 X 18 CORT SCREW SELFT    Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 4 consists of all products under  product code HWC, and same usage:  Item no:	  47482002603	2.0 X 26 CORT SCREW CRUCI  47482002803	2.0 X 28 CORT SCREW CRUCI  47482003203	2.0 X 32 CORT SCREW CRUCI  47482003403	2.0 X 34 CORT SCREW CRUCI  47482003603	2.0 X 36 CORT SCREW CRUCI  47482003803	2.0 X 38 CORT SCREW CRUCI  47482004003	2.0 X 40 CORT SCREW CRUCI  47482004203	2.0 X 42 CORT SCREW CRUCI  47482004403	2.0 X 44 CORT SCREW CRUCI  47482004603	2.0 X 46 CORT SCREW CRUCI  47482004803	2.0 X 48 CORT SCREW CRUCI  47482005003	2.0 X 50 CORT SCREW CRUCI  47482702000	2.7 X 20 CORT SCREW HEX    	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	  	Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 16 consists of all product under  poduct code: KWY and same usage:  Item no:	  500103822	BIPOLAR LINER 38MM OD X 2  500103922	BIPOLAR LINER 39MM OD X 2  500104022	BIPOLAR LINER 40/41MM OD  500104026	BIPOLAR LINER 40MM OD X 2  500104222	BIPOLAR LINER 42/43 OD X  500104226	BIPOLAR LINER 42MM OD X 2  500104428	BIPOLAR LINER 44/45/46MM  500104422	BIPOLAR LINER 44MM OD X 2  500104426	BIPOLAR LINER 44MM OD X 2  500104728	BIPOLAR LINER 47/48/49MM  500104722	BIPOLAR LINER 47MM OD X 2  500104726	BIPOLAR LINER 47MM OD X 2  500104732	BIPOLAR LINER 47MM OD X 3  500105028	BIPOLAR LINER 50/51/52MM  500105022	BIPOLAR LINER 50MM OD X 2  500105026	BIPOLAR LINER 50MM OD X 2  500105328	BIPOLAR LINER 53/54/55MM  500105322	BIPOLAR LINER 53MM OD X 2  500105326	BIPOLAR LINER 53MM OD X 2  500105728	BIPOLAR LINER 57/58MM OD  500105722	BIPOLAR LINER 57MM OD X 2  500106028	BIPOLAR LINER 60/62MM OD  500106828	BIPOLAR LINER 68/70MM OD  500106832	BIPOLAR LINER 68MM OD X 3  500107228	BIPOLAR LINER 72MM OD X 2  500103800	BIPOLAR SHELL 38MM OD  500103900	BIPOLAR SHELL 39MM OD  500104000	BIPOLAR SHELL 40MM OD  500104100	BIPOLAR SHELL 41MM OD  500104200	BIPOLAR SHELL 42MM OD  500104300	BIPOLAR SHELL 43MM OD  500104400	BIPOLAR SHELL 44MM OD  500104500	BIPOLAR SHELL 45MM OD  500104600	BIPOLAR SHELL 46MM OD  500104700	BIPOLAR SHELL 47MM OD  500104800	BIPOLAR SHELL 48MM OD  500104900	BIPOLAR SHELL 49MM OD  500105000	BIPOLAR SHELL 50MM OD  500105100	BIPOLAR SHELL 51MM OD  500105200	BIPOLAR SHELL 52MM OD  500105300	BIPOLAR SHELL 53MM OD  500105400	BIPOLAR SHELL 54MM OD  500105500	BIPOLAR SHELL 55MM OD  500105700	BIPOLAR SHELL 57MM OD  500105800	BIPOLAR SHELL 58MM OD  500106000	BIPOLAR SHELL 60MM OD  500106200	BIPOLAR SHELL 62MM OD  500107000	BIPOLAR SHELL 70MM OD    Product Usage:  For use in total or hemi hip arthroplasty
Product 24 consists of all product under  product code: HRS and same usage:  Item no:	  234703104	DISTAL MEDIAL FEMORAL CON  234703206	DISTAL MEDIAL FEMORAL CON  234703208	DISTAL MEDIAL FEMORAL CON  234800504	DISTAL POSTERIOR/LATERAL  234800506	DISTAL POSTERIOR/LATERAL  234800508	DISTAL POSTERIOR/LATERAL  234800510	DISTAL POSTERIOR/LATERAL  234800604	DISTAL POSTERIOR/LATERAL  234800606	DISTAL POSTERIOR/LATERAL  234800608	DISTAL POSTERIOR/LATERAL  234800610	DISTAL POSTERIOR/LATERAL  234800614	DISTAL POSTERIOR/LATERAL    Product Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 13 consists of all product under product code HWC  , and same usage:  Item no:	  47486510002	6.5 X 100 CANC SCREW, 32M    Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 71 consists of all product under product code: JDI and same usage:  Item no:	  783401000	VERSYS PRESS FIT LD/FX ST  783401100	VERSYS PRESS FIT LD/FX SZ  783401200	VERSYS PRESS FIT LD/FX SZ  783401300	VERSYS PRESS FIT LD/FX SZ  783401400	VERSYS PRESS FIT LD/FX SZ  783401500	VERSYS PRESS FIT LD/FX SZ  783401600	VERSYS PRESS FIT LD/FX SZ    For use in total or hemi hip arthroplasty
Product 37 consists of all product under  product code: HSB and same usage:  Item no:	  225302055	INTERLOCKING IM SCREW LG  225303055	INTERLOCKING IM SCREW LG  225304055	INTERLOCKING IM SCREW LG  225304555	INTERLOCKING IM SCREW LG  225305055	INTERLOCKING IM SCREW LG  225305555	INTERLOCKING IM SCREW LG  225306055	INTERLOCKING IM SCREW LG  225306555	INTERLOCKING IM SCREW LG  225307055	INTERLOCKING IM SCREW LG  225307555	INTERLOCKING IM SCREW LG  225308055	INTERLOCKING IM SCREW LG  225308555	INTERLOCKING IM SCREW LG  225309055	INTERLOCKING IM SCREW LG  225302542	INTERLOCKING IM SCREW MED  225303042	INTERLOCKING IM SCREW MED  225303542	INTERLOCKING IM SCREW MED  225304042	INTERLOCKING IM SCREW MED  225304542	INTERLOCKING IM SCREW MED  225305042	INTERLOCKING IM SCREW MED  225305542	INTERLOCKING IM SCREW MED  225306042	INTERLOCKING IM SCREW MED  225306542	INTERLOCKING IM SCREW MED  225307042	INTERLOCKING IM SCREW MED  225307542	INTERLOCKING IM SCREW MED  225308042	INTERLOCKING IM SCREW MED  225308542	INTERLOCKING IM SCREW MED  225302037	INTERLOCKING IM SCREW SML  225302537	INTERLOCKING IM SCREW SML  225303037	INTERLOCKING IM SCREW SML  225303537	INTERLOCKING IM SCREW SML  225304037	INTERLOCKING IM SCREW SML  225304537	INTERLOCKING IM SCREW SML  225305037	INTERLOCKING IM SCREW SML  225305537	INTERLOCKING IM SCREW SML  225306037	INTERLOCKING IM SCREW SML  225306537	INTERLOCKING IM SCREW SML  225308537	INTERLOCKING IM SCREW SML    Product Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 62 consists of all product under product code: LPH and same usage:  Item no:	  620003620	TRILOGY ACET SHELL 36MM OD MULTI    For use in total hip arthroplasty
Product 72 consists of all  product code: JDI and same usage:  Item no:	  805002202	ZIMTRON HEAD 12/14 0X22 MM     For use in total or hemi hip arthroplasty
Product 70 consists of all product under product code: JDI and same usage:  Item no:	  785701000	VERSYS HERITAGE FEM STEM  785701100	VERSYS HERITAGE FEM STEM  785701200	VERSYS HERITAGE FEM STEM  785701300	VERSYS HERITAGE FEM STEM  785701320	VERSYS HERITAGE FEM STEM  785701400	VERSYS HERITAGE FEM STEM  785701420	VERSYS HERITAGE FEM STEM  785701500	VERSYS HERITAGE FEM STEM  785701520	VERSYS HERITAGE FEM STEM  785701600	VERSYS HERITAGE FEM STEM  785701700	VERSYS HERITAGE FEM STEM    For use in total or hemi hip arthroplasty
Product 34 consists of all product under  product code: JWH and same usage:  Item no:	  522001700	I/B II KNEE DOMED PATELLA  522001800	I/B II KNEE DOMED PATELLA  522001900	I/B II KNEE DOMED PATELLA  for use in total knee arthroplasty
Product 54 consists of all product under product code: JWH and same usage:  Item no:	  596009900	NEXGEN TAPER PLUG  for use in total knee arthroplasty
Product 57 consists of all product code: JDI and same usage:  Item no:	  763401000	PRESSFIT FEM ST FX 10 X 115  763401100	PRESSFIT FEM ST FX 11 X 1  763401200	PRESSFIT FEM ST FX 12 X 1  763401300	PRESSFIT FEM ST FX 13 X 1  763401400	PRESSFIT FEM ST FX 14 X 1  763401500	PRESSFIT FEM ST FX 15 X 1    For use in total or hemi hip arthroplasty
Product 1 consists of all product under  , product code: JWH and same usage:  Item no:	  47481500601	1.5 X 6 CORT SCREW HEX/SE  Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 51 consists of all product under  product code: JWH and same usage:  Item no:	  598603701	NEXGEN OPTION STEMMED TIB  598603702	NEXGEN OPTION STEMMED TIB  598604701	NEXGEN OPTION STEMMED TIB  598604702	NEXGEN OPTION STEMMED TIB  598605701	NEXGEN OPTION STEMMED TIB  598605702	NEXGEN OPTION STEMMED TIB    for use in total knee arthroplasty
Product 8 consists of all products under product code HWC, and same usage:  Item no:	  47483501201	3.5MM CORT. SCREW 12MM LN  47483501401	3.5MM CORT. SCREW 14MM LN  47483501601	3.5MM CORT. SCREW 16MM LN  47483501801	3.5MM CORT. SCREW 18MM LN  47483503601	3.5MM CORT. SCREW 36MM LN  47483507501	3.5MM CORT. SCREW 75MM LN  	  Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 23 consists of all product code: JDI and same usage:  Item no:	  801100220	CPT 2 HIP STEM, X-OFFSET  801100320	CPT 3 HIP STEM, X-OFFSET  801100420	CPT 4 HIP STEM, X-OFFSET  801100005	CPT HIP STEM PETITE  801100700	CPT HIP STEM SZ 2 LONG  801100800	CPT HIP STEM SZ 3 LONG  801100222	CPT MOD HD ST/ST 22MED SH  801100322	CPT MOD HD ST/ST 22MMD LN  801100122	CPT MOD HD ST/ST 22MMD SH  801100126	CPT MOD HD ST/ST 26MMD SH  801100328	CPT MOD HD ST/ST 28MMD LN  801100228	CPT MOD HD ST/ST 28MMD ME  801100128	CPT MOD HD ST/ST 28MMD SH  801100332	CPT MOD HD ST/ST 32MMD LN  801100232	CPT MOD HD ST/ST 32MMD ME  801100132	CPT MOD HD ST/ST 32MMD SH  801100100	CPT MODULAR STEM SIZE 1 S  801100200	CPT MODULAR STEM SIZE 2 S  801100300	CPT MODULAR STEM SIZE 3 S  801100400	CPT MODULAR STEM SIZE 4 S  801100500	CPT MODULAR STEM SIZE 5 S  For use in total or hemi hip arthroplasty
Product 38 consists of all product under  product code: HSB and same usage:  Item no:	  225303255	INTERLOCKING IM SCREW LG  225303555	INTERLOCKING IM SCREW LG  225303755	INTERLOCKING IM SCREW LG  225307055	INTERLOCKING IM SCREW LG  225302742	INTERLOCKING IM SCREW MED  225303242	INTERLOCKING IM SCREW MED  225307042	INTERLOCKING IM SCREW MED  225302737	INTERLOCKING IM SCREW SML  225303237	INTERLOCKING IM SCREW SML    Product Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 11 consists of all product under product code JDI  , and same usage:  Item no:	  902602500	6 DEGREE COCR FEM HEAD 26  902602600	6 DEGREE COCR FEM HEAD 26  902602700	6 DEGREE COCR FEM HEAD 26  902602800	6 DEGREE COCR FEM HEAD 28  902602900	6 DEGREE COCR FEM HEAD 28  902603000	6 DEGREE COCR FEM HEAD 28  902603300	6 DEGREE COCR FEM HEAD 32  902603200	6 DEGREE COCR FEM HEAD 32  	  Product Usage:  For use in total or hemi hip arthroplasty
Product 56 consists of all product under product code: HWC and same usage:  Item no:	  47234702032	PERI SCR 3.5MM X 32MM STE  47234702018	PERI SCR. 3.5MM X 18MM ST  47234702020	PERI SCR. 3.5MM X 20MM ST  47234702022	PERI SCR. 3.5MM X 22MM ST  47234702026	PERI SCR. 3.5MM X 26MM ST  47234702030	PERI SCR. 3.5MM X 30MM ST  47234702034	PERI SCR. 3.5MM X 34MM ST  47234702036	PERI SCR. 3.5MM X 36MM ST  47234702042	PERI SCR. 3.5MM X 42MM ST  47234702046	PERI SCR. 3.5MM X 46MM ST  47234702050	PERI SCR. 3.5MM X 50MM ST  47234702080	PERI SCR. 3.5MM X 80MM ST  47234702085	PERI SCR. 3.5MM X 85MM ST  47234702155	PERI SCR. 4.0MM X 55MM  47234702160	PERI SCR. 4.0MM X 60MM  47234702210	PERI SCR. 4.0MMX10MM FULL  47234702212	PERI SCR. 4.0MMX12MM FULL  47234702214	PERI SCR. 4.0MMX14MM FULL  47234702216	PERI SCR. 4.0MMX16MM FULL  47234702260	PERI SCR. 4.0MMX60MM FULL  47234702336	PERI SCR. 4.5MM X 36MM  47234702338	PERI SCR. 4.5MM X 38MM  47234712440	PERI SCR. 6.5MM X 140MM  47234702670	PERI SCR. 6.5MM X 70MM  47234702122	PERI. SCR 4.0MM X22MM  47234702124	PERI. SCR 4.0MM X24MM  47234702126	PERI. SCR 4.0MM X26MM  47234702128	PERI. SCR 4.0MM X28MM    Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 53 consists of all product under:    product code: JWH and same usage:  Item no:	  597002501	NEXGEN PRECOAT PEG TIB PL  597002502	NEXGEN PRECOAT PEG TIB PL  597003501	NEXGEN PRECOAT PEG TIB PL  597003502	NEXGEN PRECOAT PEG TIB PL  597004501	NEXGEN PRECOAT PEG TIB PL  597004502	NEXGEN PRECOAT PEG TIB PL  597005501	NEXGEN PRECOAT PEG TIB PL  597005502	NEXGEN PRECOAT PEG TIB PL  597005503	NEXGEN PRECOAT PEG TIB PL  597005504	NEXGEN PRECOAT PEG TIB PL  598002701	NEXGEN PRECOAT STEMMED TI  598002702	NEXGEN PRECOAT STEMMED TI  598003701	NEXGEN PRECOAT STEMMED TI  598003702	NEXGEN PRECOAT STEMMED TI  598004701	NEXGEN PRECOAT STEMMED TI  598004702	NEXGEN PRECOAT STEMMED TI  598005701	NEXGEN PRECOAT STEMMED TI  598005702	NEXGEN PRECOAT STEMMED TI  598005703	NEXGEN PRECOAT STEMMED TI  598005704	NEXGEN PRECOAT STEMMED TI  598801510	NEXGEN SHARP FLUTED STEM  598801511	NEXGEN SHARP FLUTED STEM  598801512	NEXGEN SHARP FLUTED STEM  598801513	NEXGEN SHARP FLUTED STEM  598801514	NEXGEN SHARP FLUTED STEM  598801515	NEXGEN SHARP FLUTED STEM  598801516	NEXGEN SHARP FLUTED STEM  598801517	NEXGEN SHARP FLUTED STEM  598801518	NEXGEN SHARP FLUTED STEM  598801519	NEXGEN SHARP FLUTED STEM  598801520	NEXGEN SHARP FLUTED STEM  598801010	NEXGEN STRAIGHT STEM EXT  598801011	NEXGEN STRAIGHT STEM EXT  598801012	NEXGEN STRAIGHT STEM EXT  598801013	NEXGEN STRAIGHT STEM EXT  598801014	NEXGEN STRAIGHT STEM EXT  598801015	NEXGEN STRAIGHT STEM EXT  598801016	NEXGEN STRAIGHT STEM EXT  598801017	NEXGEN STRAIGHT STEM EXT  598801018	NEXGEN STRAIGHT STEM EXT  598801020	NEXGEN STRAIGHT STEM EXT  598801022	NEXGEN STRAIGHT STEM EXT  598801024	NEXGEN STRAIGHT STEM EXT  598801112	NEXGEN STRAIGHT STEM EXT  598801113	NEXGEN STRAIGHT STEM EXT  598801114	NEXGEN STRAIGHT STEM EXT  598801115	NEXGEN STRAIGHT STEM EXT  598801116	NEXGEN STRAIGHT STEM EXT  598801117	NEXGEN STRAIGHT STEM EXT  598801118	NEXGEN STRAIGHT STEM EXT  598801212	NEXGEN STRAIGHT STEM EXT  598801215	NEXGEN STRAIGHT STEM EXT    for use in total knee arthroplasty
Product 14 consists of all product under  product code HSB  , and same usage:  Item no:	  225600230	ASIA ONE-PIECE LAG SCREW  225600232	ASIA ONE-PIECE LAG SCREW  225600235	ASIA ONE-PIECE LAG SCREW  225600237	ASIA ONE-PIECE LAG SCREW  225600240	ASIA ONE-PIECE LAG SCREW  225600242	ASIA ONE-PIECE LAG SCREW  225600245	ASIA ONE-PIECE LAG SCREW  225600227	ASIA ONE-PIECE LAG SCREW 70MM    Product Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.
Product 5 consists of all products under  product code HWC, and same usage:  Item no:	  	  47482701001	2.7MM CORT. SCREW 10MM, S  47482701201	2.7MM CORT. SCREW 12MM, S  47482701401	2.7MM CORT. SCREW 14MM, S  47482701601	2.7MM CORT. SCREW 16MM, S  47482701801	2.7MM CORT. SCREW 18MM, S  47482702001	2.7MM CORT. SCREW 20MM, S  	  	  	Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 2 consists of all products product code LPH, and same usage:  801802202	12/14 COCR FEMORAL HEAD 2  801802220	12/14 COCR FEMORAL HEAD 2  801802230	12/14 COCR FEMORAL HEAD 2  801802601	12/14 COCR FEMORAL HEAD 2  801802602	12/14 COCR FEMORAL HEAD 2  801802603	12/14 COCR FEMORAL HEAD 2  801802604	12/14 COCR FEMORAL HEAD 2  801802605	12/14 COCR FEMORAL HEAD 2  801802801	12/14 COCR FEMORAL HEAD 2  801802802	12/14 COCR FEMORAL HEAD 2  801802803	12/14 COCR FEMORAL HEAD 2  801802805	12/14 COCR FEMORAL HEAD 2  801802814	12/14 COCR FEMORAL HEAD 2  801803201	12/14 COCR FEMORAL HEAD 3  801803202	12/14 COCR FEMORAL HEAD 3  801803203	12/14 COCR FEMORAL HEAD 3  801803205	12/14 COCR FEMORAL HEAD 3  801803214	12/14 COCR FEMORAL HEAD 3  801803601	12/14 COCR FEMORAL HEAD 3  801803602	12/14 COCR FEMORAL HEAD 3  801803603	12/14 COCR FEMORAL HEAD 3  801803604	12/14 COCR FEMORAL HEAD 3  801803605	12/14 COCR FEMORAL HEAD 3  801804001	12/14 COCR FEMORAL HEAD 4  801804002	12/14 COCR FEMORAL HEAD 4  801804003	12/14 COCR FEMORAL HEAD 4  801804004	12/14 COCR FEMORAL HEAD 4  902602100	6 DEGREE COCR FEM HEAD 22  32902603935	FEM HD 26MMDIA SHT NK+  32902603800	FEMORAL HEAD +0.5 X 22 MM  32902604810	FEMORAL HEAD +3.5 X 22 MM  32902604845	FEMORAL HEAD +7.0 X 22 MM  For use in total or hemi hip arthroplasty
Product 9 consists of all product under HRS, and same usage:  Item no:	  47494502601	4.5 BROAD SCP PLT, 26 HOL  	  	  	  Product Usage:  Temporary internal fixation devices designed to stabilize fractures during the normal healing process.
Product 7 consists of all products under  product code HWC, and same usage:  Item no:	  47234801435	3.5MM CORT SCR X 14MM  47234801635	3.5MM CORT SCR X 16MM  47234806535	3.5MM CORT SCR X 65MM  47234807035	3.5MM CORT SCR X 70MM  47234807535	3.5MM CORT SCR X 75MM  47234808035	3.5MM CORT SCR X 80MM  47234808535	3.5MM CORT SCR X 85MM  47234809035	3.5MM CORT SCR X 90MM  Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 20 consists of all prod oct under  poduct code: KTT and same usage:  Item no:	  47116201900	COMPRESSION SCREW 1/2IN  47116202300	COMPRESSION SCREW 1-1/2IN  47116202200	COMPRESSION SCREW 1-1/4IN  47116202400	COMPRESSION SCREW 1-3/4IN  47116202100	COMPRESSION SCREW 1IN  47116202000	COMPRESSION SCREW 3/4IN    Product Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
Product 26 consists of all product under  product code: JWH and same usage:  Item no:	  234703104	DISTAL MEDIAL FEMORAL CON  234703206	DISTAL MEDIAL FEMORAL CON  234703208	DISTAL MEDIAL FEMORAL CON  234800504	DISTAL POSTERIOR/LATERAL  234800506	DISTAL POSTERIOR/LATERAL  234800508	DISTAL POSTERIOR/LATERAL  234800510	DISTAL POSTERIOR/LATERAL  234800604	DISTAL POSTERIOR/LATERAL  234800606	DISTAL POSTERIOR/LATERAL  234800608	DISTAL POSTERIOR/LATERAL  234800610	DISTAL POSTERIOR/LATERAL  234800614	DISTAL POSTERIOR/LATERAL      Product Usage:  For use in total or hemi hip arthroplasty
Product 3 consists of all products under product code JDI, and same usage:  Item no:781803800	12/14 UNIPOLAR FEMORAL HE  781804000	12/14 UNIPOLAR FEMORAL HE  781804100	12/14 UNIPOLAR FEMORAL HE  781804200	12/14 UNIPOLAR FEMORAL HE  781804300	12/14 UNIPOLAR FEMORAL HE  781804400	12/14 UNIPOLAR FEMORAL HE  781804500	12/14 UNIPOLAR FEMORAL HE  781804600	12/14 UNIPOLAR FEMORAL HE  781804700	12/14 UNIPOLAR FEMORAL HE  781804800	12/14 UNIPOLAR FEMORAL HE  781804900	12/14 UNIPOLAR FEMORAL HE  781805000	12/14 UNIPOLAR FEMORAL HE  781805100	12/14 UNIPOLAR FEMORAL HE  781805200	12/14 UNIPOLAR FEMORAL HE  781805300	12/14 UNIPOLAR FEMORAL HE  781805400	12/14 UNIPOLAR FEMORAL HE  781805500	12/14 UNIPOLAR FEMORAL HE  781806300	12/14 UNIPOLAR FEMORAL HE  781809900	12/14 UNIPOLAR FEMORAL HE  781809901	12/14 UNIPOLAR FEMORAL HE  781809902	12/14 UNIPOLAR FEMORAL HE    Product For use in total or hemi hip arthroplasty
Product 50 consists of all product under  product code: JWH and same usage:  Item no:	  595002701	NEXGEN MIS TIBIA PLATE PR  595002702	NEXGEN MIS TIBIA PLATE PR  595003701	NEXGEN MIS TIBIA PLATE PR  595003702	NEXGEN MIS TIBIA PLATE PR  595003712	NEXGEN MIS TIBIA PLATE PR  595004701	NEXGEN MIS TIBIA PLATE PR  595004702	NEXGEN MIS TIBIA PLATE PR  595005701	NEXGEN MIS TIBIA PLATE PR  595005702	NEXGEN MIS TIBIA PLATE PR    for use in total knee arthroplasty
Product 41 consists of all product under  product code: KTT and same usage:  Item no:	  119301042	LAG SCR 12.7D X 100MM STA  119301045	LAG SCR 12.7D X 105MM STA  119301047	LAG SCR 12.7D X 110MM STA  119301050	LAG SCR 12.7D X 115MM STA  119301052	LAG SCR 12.7D X 120MM STA  119301055	LAG SCR 12.7D X 125MM STA  119301057	LAG SCR 12.7D X 130MM STA  119301060	LAG SCR 12.7D X 135MM STA  119301062	LAG SCR 12.7D X 140MM STA  119301070	LAG SCR 12.7D X 155MM STA  119301020	LAG SCR 12.7D X 55MM STAN  119301022	LAG SCR 12.7D X 60MM STAN  119301025	LAG SCR 12.7D X 65MM STAN  119301027	LAG SCR 12.7D X 70MM STAN  119301030	LAG SCR 12.7D X 75MM STAN  119301032	LAG SCR 12.7D X 80MM STAN  119301035	LAG SCR 12.7D X 85MM STAN  119300537	LAG SCR 12.7D X 90MM SHOR  119301037	LAG SCR 12.7D X 90MM STAN  119301040	LAG SCR 12.7D X 95MM STAN  119301542	LAG SCR 15.8D X 100MM LAR  119301545	LAG SCR 15.8D X 105MM LAR  119301547	LAG SCR 15.8D X 110MM LAR  119301550	LAG SCR 15.8D X 115MM LAR  119301552	LAG SCR 15.8D X 120MM LAR  119301555	LAG SCR 15.8D X 125MM LAR  119301557	LAG SCR 15.8D X 130MM LAR  119301520	LAG SCR 15.8D X 55MM LARG  119301522	LAG SCR 15.8D X 60MM LARG  119301525	LAG SCR 15.8D X 65MM LARG  119301532	LAG SCR 15.8D X 80MM LARG  119301535	LAG SCR 15.8D X 85MM LARG  119301537	LAG SCR 15.8D X 90MM LARG    Product Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical
Chocolate Chile Pecan Mini Miracle Tart 4.87 oz (138g) NET WT Party Pack of 6 in formed plastic tray
List of ingredient fails to include almond flour.
NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-134-61
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61
CJ Extra Fancy Long Grain Enriched Rice.  NET WT. 80 lbs (36.20 kg);  nylon bag;  Product of USA.  Item number RG80
15  x 80 lb. bags (7 bags already returned)
FDA inspection found rodent urine stains on pallets of long grain rice in 80 lb. bags.
Lot numbers #873, #876, #878. These numbers are according to supplier information on pallets; bags to not have lot numbers.
NABUMETONE Tablets USP, 750 mg, 100 count bottle,Teva Pharmaceutical Industries Ltd., Jerusalem, 91010, ISRAEL
Labeling: Not Elsewhere Classified: Lack of leaflets and approved labels on bottles.
Worldwide distribution.  US nationwide, Australia, Bahrain, Bulgaria, Canada, Greece, Italy, Malaysia, Mexico, Qatar, Russia, Spain, and United Kingdom.
Quick Connects. Steris Corporation.  Model numbers: QKC1736E, QKC1736INT, QKC1737E, and QKC1737INT. Each Quick Connect contains a flow unit consisting of tubing, tethers, and adapters. For sterilant and rinse water used in endoscope washers.
The firm discovered that one of the hysteroscope models listed for processing in four existing Quick Connects has one inlet port rather than two inlet ports as indicated in the Quick Connect processing instructions.
All Lots. Model numbers: QKC1736E, QKC1736INT, QKC1737E, and QKC1737INT.
Battery Pack  KLS-SD-1000  Single  Models: KLS-BP-001  Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
The sterile battery may contain particulates within the sterile package.
Battery Pack  KLS-SD-1000  Case (40 ct)  Models: KLS-BP-040    Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
Covidien LP (formerly Nellcor Puritan Bennett Inc.)
Worldwide Distribution -- US, including but not limited to the territory of Puerto Rico; and Ireland, Jordan, Saudi Arabia, Bahrain, Australia, Japan, Israel, Turkey, Chile, South Africa, Costa Rica, United Arab Emirates, Qatar, Peru, Panama, Singapore, Kuwait,  Lebanon, Brazil, Mexico, Colombia, Russia, Uruguay, Slovenia, Morocco, Argentina, Egypt, and Romania.
Puritan Bennett 980 Ventilator System, PB980 Ventilator (980xxxxxxxx).    Intended to provide continuous ventilation for pediatric and adult patients who require either invasive ventilation or non-invasive ventilation.
Graphical user interface (GUI) unresponsive to touch and Loss of primary ventilation under certain circumstances.  Covidien Respiratory and Monitoring Solutions, now a part of Medtronic, issued a field corrective action notice for two issues on all models of Puritan Bennett 980 (PB980) ventilator.
Worldwide Distribution - US Distribution to the states of : AZ, CA, FL, IA,  ID,  IL, MA, , MN, MT and ND., and to the countries of Canada, France and Hong Kong.
Sekure Chemistry Sekisui  Diagnostics Acetaminophen L3K Assay, In-vitro Diagnostic  Catalog Number: 506-10: R1: 1 x 10ml, R2: 2 x 10ml  Catalog Number: 506-30: R1: 3 x 10ml, R2: 6 x 10ml    In-Vitro quantitative measurement of Acetaminophen in serum and plasma used m the diagnosis and treatment of acetaminophen overdose toxicity.
Crystal formation in the Color Reagent (R2) when left on board automated analyzers causing samples to under recover
Blood product, in which quality control and failure to quarantine unit due to medical history, was distributed.
US Nationwide Distribution including states of:AL, AZ, CA, CO, CT, FL, GA, IN, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ,NY, OH, OR, PA, RI, TN, TX, VA, WA, WV, and Hawaii.
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM    The product includes a Catheter Sheath Introducer (CSI) and a vessel dilator. A Catheter Sheath Introducer facilitates percutaneous entry of an intravascular device. A vessel dilator facilitates the percutaneous entry of the CSI by forming an atraumatic transition from the skin through the subcutaneous tissue to the vessel.
Incorrect cannula of the sheath introducer (smaller than intended).
NuOss XC Sinus  Reference No 509-3001 (BMCU17, size 17 mm diameter x 10 mm height)  Reference No 509-3002 (BMCU22, size 22 mm diameter x 12 m height)    Manufacturer:- Collagen Matrix,   Distributor:- ACE Surgical Supply Co, Inc,     Intended use for dental surgery such as -augmentation or reconstructive treatment of alveoloar ridge -filling of infrabony periodontal defects -filling of defects after root resection, apicoectomy and cystectomy -filling of extraction sockets to enhance preservation of the alveolar ridge -elevation of maxillary sinus floor -filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) -Filling of pre-implant defects in conjunction with products intended for Guided Bone Regeneration
During the 36 month real time shelf life testing of NuOss XC Sinus (BMCU-Umbrella) to verify the 3 year shelf life designated for the device, 3 of 13 products did not pass the recovery test, which requires that the compressed product fully expand within 1 minute of hydration time.
Lot BMCXU11P1. BMCXU11H3    Lot BMCXU11P1, BMCXU12P1
ZCORE Porcine Xenograft Particulate in Syringe    Product Intended for use in dental surgery such as:  -Augmentation or reconstructive treatment of alveolar ridge  -filling of defects after root resection, apicoectomy and cystectomy  -Filling of extraction sockets to enhance preservation of the alveolar ridge  -elevation of maxillary sinus floor  -Filling of periodontal defects in conjunction with products  -Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)  -Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration.
The distributor, Osteogenics Biomedical,  notified the firm that the syringes were not working properly and the syringes were being held in quarantine.
PMCS025     Lot No. PMCSU15A1    PMCS05    Lot No. PMCSU15A1      PMCS10    Lot No. PMCSU15A1    PMCS05    Lot No. PMCSU15A2        PMCS10  Lot No. PMCSU15A2
Worldwide Distribution - US (Virginia only) Internationally to Canada, France & Indonesia.
Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602  for use as diagnostic contact lenses for eye examinations (including the anterior chamber, trabecular meshwork, central retina, and peripheral retina) and use in the therapy of intraocular abnormalities
The firm discovered that the incorrect lot number was engraved on the product.
Blood product, collected within a year from a donor who lived in a malarial endemic area, was distributed.
NuOSS Cancellous    Intended for use in dental surgery.
On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of NuOss Cancellous product shipped to a distributor may have included an incorrect size.
Reference No. BM2C20010-U  Lot no. BM2CU15E2
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
Nationwide Distribution including AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, TN, TX, UT, VA, WA, WI, and WV.
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System  Accu-Chek inform II Blood Glucose Monitoring System is intended for testing outside the body (in vitro diagnostic use) and is intended for multiple-patient use in professional healthcare settings. This system should only be use with single-use, auto-disabling lancing devices.
Accu-Chek Inform II Base Unit might produce physical transmission errors in the form of data loss in the communication between the meter and the Data Management Systems (DMS). The issue can lead to the data loss or in the worst case to an erroneous assignment of the patient data (patient mismatch). The issue will only occur at sites using POTCT1-A communication via USB.
Model/Catalog/Part Number: 05060290001; serial numbers: UU41000000 through UU41064963 and UU41064964 through  UU41122741.
Pilling Modular Verres Body/Obturator, Product Code 140880
Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).
Blood and Blood Products for Reprocessing
Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Morning Star Disaster Supplies Quick Meal  Mexican Corn Soup Mix Net Wt. 8.1 oz (230g)., Foil Bag.  UPC 853328-006090      Wilderness Family Naturals  Quick Meal  Mexican Corn Soup Mix., Net Wt 8.1 oz (230 g)., Foil Bag. UPC 898392-007949
Wilderness Family Naturals Organic Coconut Milk Powder and other products that contain this as an ingredient are being recalled  due to potential milk contamination.
Morning Star Disaster Supplies ,Creamy Potato Corn Chowder, Net Wt. 7.88 oz (223 g).  UPC 853328-006052, Foil Bag     Wilderness Family Naturals  Quick Meal  Potato Corn Chowder, Net Wt 7.88 oz (223 g). UPC 853328-006199, Foil Bag
Wilderness Family Naturals Coconut Chia Pudding Mix Organic, packaged in the following sizes:    1.1 lb Plastic Bag, UPC 898392-007789, and 13.2 lb.  (12 plastic bags in a cardboard box) UPC 01002466
Wilderness Family Naturals Coconut Milk, Powdered, Organic packaged in the following sizes:    1) 16 oz foil pouch, UPC 98392-00769;  2)  12 lb. Case of 12 - 1 lbs packages, UPC 01002457  3) 5 lb. bag, UPC 98392-00770  4) 30 lb. Case of 6 - 5 lb. packages, UPC 01002458  5)  Case of 1-55 lb. package, UPC 01002459  6) Trial Sample size, UPC 01002463
Wilderness Family Naturals Cacao, Organic Hot Chocolate Mix Packaged in the following sizes:  1 lb. Foil Bag, UPC 898392-007765;    12 lb. (12 - 1 lb. Foil Bags in a cardboard box), UPC 01002464;    5 lb. Foil Bag, UPC 898392-007772;  and   30 lb. (6-5lb. Foil Bags in a cardboard box), UPC 01002465
Wilderness Family Naturals Mango Raspberry Cereal  Organic  8 oz., Foil Bag.    UPC 898392-007826.
Wilderness Family Naturals Choco Maca Strawberry Cereal  Organic  8 oz.., Foil Bag    UPC 898392-007819
Morning Star Disaster Supplies  Jamaican Beans and Rice, Net Wt 8.62 oz (244 g). UPC 853328-006076, Foil Bag    Wilderness Family Naturals Quick Meal  Jamaican Beans and Rice, Net Wt 8.62 oz (244 g). UPC 898392-007987, Foil Bag
Morning Star Disaster Supplies  Butternut Squash Soup, Net Wt 4.75oz (135 g).  UPC 853328-006113, Foil Bag    Wilderness Family Naturals Quick Meal  Butternut Squash Soup, Net Wt 4.75 oz (135 g). UPC 853328-006182, Foil Bag
Morning Star Disaster Supplies Coconut Vegetable Curry over Quinoa, Net Wt 4.95 oz (115 g). UPC 853328-006069, Foil Bag    Wilderness Family Naturals  Quick Meal  Coconut Vegetable Curry over Quinoa,  Net Wt 4.95 oz (115 g). UPC 853328-006229, Foil Bag
Morning Star Disaster Supplies  Creamy Coconut Rice Soup, Net Wt 7.25 oz (206 g). UPC 853328-006038, Foil Bag    Wilderness Family Naturals  Quick Meal  Creamy Coconut Rice Soup, Net Wt  7.25 oz (206 g). UPC 853328-006038, Foil Bag
Morning Star Disaster Supplies Broccoli Potato Soup Mix, Net Wt 6.91 oz (196 g). UPC 853328-006014, Foil Bag    Wilderness Family Naturals  Quick Meal  Broccoli Potato Soup Mix, Net Wt 6.91, (196 g). UPC 898392-007963, Foil Bag
Wilderness Family Naturals Coconut Chia Pudding Mix  Sweetened with Coconut Sap Sugar  Organic  Packaged in the following sizes:  1.1 lb. Plastic Bag, UPC 898392-007796 and 13.2 lb. (12 Plastic Bags in a cardboard box), UPC  01002467
Morning Star Disaster Supplies Tomato Basil Soup, Net Wt 3.88 oz (110 g),   UPC 853328-006120, Foil Bag    Wilderness Family Naturals  Quick Meal  Tomato Basil Soup, Net Wt 3.88 oz (110 g). UPC 853328-006243, Foil Bag
Morning Star Disaster Supplies Creamy Mushroom Wild Rice Soup, Net Wt 7.3 oz (207 g). UPC 853328-006045, Foil Bag    Wilderness Family Naturals  Quick Meal  Creamy Mushroom Wild Rice Soup Mix, Net Wt 7.3 oz (207 g). UPC 898392-007994, Foil Bag
Wilderness Family Naturals Banana Blueberry Cereal  Organic  8 oz.., Foil Bag    UPC 898392-007833
Dawn's Deviled Egg Potato Salad, Net Wt. 15 oz. (397g), UPC 32345-10107. Keep Refrigerated.
Dawn's Foods is recalling Dawn's Deluxe Potato Salad and Dawn's Deviled Egg Potato Salad due to mis-labeling and potential undeclared milk, wheat and soy.  Some containers labeled as Dawn's Deluxe Potato Salad may inadvertently contain Dawn's Deviled Egg Potato Salad, which contains soy and wheat.  Some containers of Dawn's Deviled Egg Potato Salad may inadvertently contain Dawn's Deluxe Macaroni
Dawn's Deluxe Potato Salad, Net Wt. 15 oz. (425g), UPC 32345-10015. Keep Refrigerated.
TX, GA, WY, CA, CO, MA, NH, FL, NY, AZ, MT
Faye's Texas Naturals Chili Petin Pepper Sauce Net Wt. 2 fl. oz./.59 ml in glass jars; South Courthouse Square Goliad, Texas 77963 1-800-231-FAYE
pH for the products were not tested and recorded as required by acidified food regulation.
Faye's Texas Naturals Chili Petin Picante Muy Caliente Net Wt. 16 oz./452 grams in glass jars; 123 S. Courthouse Square Goliad, Texas 77963 (361)645-3136 FAYESTEXASNATURALS.NET
Faye's Texas Naturals Chili Petin Picante Caliente Net Wt. 16oz./452 grams in glass jars; 123 S. Courthouse Square Goliad, Texas 77963 (361)645-3136 FAYESTEXASNATURALS.NET
Faye's Texas Naturals Chili Petin Corn Relish Net Wt. 10 oz./283.59 grams in glass jars; 123 S. Courthouse Square Goliad, Texas 77963 (361)645-3136 FAYESTEXASNATURALS.NET
Apheresis Red Blood Cells, Leukocytes Reduced
Blood product, collected from a donor whose suitability to donate were not adequately determined, were distributed.
Blood product, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.
American National Red Cross Great Lakes Region
Apheresis Platelets, Leukocytes Reduced, Irradiated
Blood products, which were labeled as leukoreduced, but were not tested to verify the White Blood Cell count, were distributed.
Oxygen, Compressed USP (Gaseous, Medical Oxygen, Aluminum Cylinders), Packaged in a) M6-Tanks, b) D-Tanks, and c) E-Tanks, Rx Only.  Medical Park Homecare, 139 SE Katherine Ave., Bartlesville, OK 74006.
a) 289 M6-Tank Cylinders, b) 49 D-Tank Cylinders, c) 743 E-Tank Cylinders.
CGMP Deviations: Cylinders filled using out of date gauges.
Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By: Pharmaceutics International, Inc., Hunt Valley, MD 21031, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-7656-56.
Failed Impurities/Degradation Specifications: Out of specification test results for impurities during stability testing.
NatureBox Cinnamon Yogurt Mini Grahams, 6 oz. (170g) customer stand up pouches.    UPC 8 58590 00528 4    Ingredients: Graham Crackers (unbleached unenriched wheat flour, whole wheat graham flour, sugar, palm and palm kernel oil, molasses, honey, salt, sodium bicarbonate). Yogurt Coating (sugar, palm kernel and/or palm oil, whey powder, Dry nonfat yogurt, soy lecithin (an emulsifier) salt, vanilla extract) Cinnamon.    Contains:Wheat, Milk and Soy.    Packed in a facility that also processes tree nuts, peanuts, milk, wheat, egg, soy and fish.    Distributed by:  Nature Box  San Carlos, CA 94070
Third party warehouse discovered that they found bags of Cinnamon Yogurt Mini Graham products that were packaged in Probiotic Power Mix bags. Probiotic bags do not properly declare wheat as an allergen.
Worldwide Distribution - US Nationwide, VA/govt/military
On August 15, 2012, Sorin informed consignees via letter of changes made to create Version 12 of the Heater-Cooler 3T IFU. The revised IFU included enhancements to achieve water quality that meets the standard for German drinking water.
All Serial Numbers for  Item Number 16-02-81, 16-02-82, 16-02-85;
Stryker Medical Division of Stryker Corporation
Distributed in DC and the states of AL, CA, FL, MN, MT, NC, NE, NY, PA, RI, TN, TX, UT, and WV.
Transport Stretcher, and Head and Neck Surgery Stretcher    Non-powered stretcher
The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) were manufactured using the incorrect oil. The oil used does not contain the same wear resistance additives as the specified oils and therefore its use increases the potential for wear which may cause a leak event or jack drift. Testing was done to evaluate the jacks with incorrect oil and leak events we
The hydraulic jack assemblies (Part numbers: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) used as service parts on Stretchers assembled from 8/28/15 - 8/29/15
Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom)    Powered stretcher
Worldwide Distribution -- US, including the states of CA, CT, FL, GA, IL, IN, MD, MA, MN, MO, NH, NC, OH, OR, PA, TX, UT, VA, and WI; and ,countries of CHINA, CANADA, AUSTRALIA, FRANCE, JAPAN, and GERMANY.
Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S.    Indicated for use as a magnetic resonance diagnostic device (MRDD).
Emergency helium venting lines (i.e. quench lines) may not have been properly installed.
Distributed US (nationwide) and in Canada.
The Spirit TM Select bed is a Med-Surg bed intended to support and transport  low to moderate acuity patients in the medical and/or surgical area of the hospital. The Spirit Select bed is also intended for use as a general purpose, variable height hospital bed for general care, post-operative and general medicine wards. The product has a 500 pound safe working load and includes the standard features of an integrated scale and bed exit system, enhanced footboard staff controls for scale and bed exit system and a low bed height of 10.75 inches.
Utah, Idaho, Montana, Nevada, Wyoming, Washington. No foreign or VA/govt/military consignees.
ice cream which presents a potential allergen threat.
Covidien Medical Products (Shanghai) Manufacturing L.L.C.
Worldwide Distribution - US Nationwide, VA/govt/military consignees.
Technology    Product Usage:  The Covidien Emprint Ablation System is intended for use in percutaneous,laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of non-resectable liver tumors. The CovidienEmprint Ablation System is not intended for use in cardiac procedures
Model Numbers: CA15L1, CA20L1 and CA30L1
Worldwide Distribution - USA (nationwide) including Puerto Rico and to the states of : AL, AK, AZ, AR, CA, CO, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OR, PA, RI, SC, TN, TX, VT, VA, WA, WV, WI, WY.,  and the countries of : Guam, Great Britain, France, Canada, Ireland and Australia
McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products 12.0 and 12.1.1.
McKesson has identified a design deficiency where under rare circumstances, imported images/studies may re-use a non-unique image directory.  This issue may cause incorrect images to be displayed for a patient.
Citrus Flavored Soda Mello Yello, 12 fl. oz. (355 ml), Canned under authority of The Coca-Cola Company, Atlanta, GA 30313, UPC 497250
US Nationwide Distribution including states of: MN, NC, NE, FL, TX, CA, AR, MI, MA, IL, DE, VA, SC, OH, CO, WI, MO, NY, CT, UT, PA, WA, NJ, GA, IN, MD, TN, LA, OR, AZ, ND, KS, AL, NM.
Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637, 10091673      intended for acceptance, transfer, display, storage, archive acceptance, transfer, display, storage, archive and manipulation of digital medical images, including quantification and report generation. Not intended for reading of mammography images.
Siemens' conducting a recall due to a potential issue when using the measurement package of the VA10 version of syngo Dynamics.
Virt-Nate Prenatal/Postnatal, Prescription Folate-Containing Dietary Supplement, Rx, 100 count bottles, Manufactured For: Virtus Pharmaceuticals, Tampa, FL
Tablets/Capsules Imprinted with Wrong ID; product debossed with an incorrect punch. Bottles could contain tablets debossed with V259 (debossing for PreTab) instead of the correct punch, V264 (debossing for Virt-Nate).