Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Worldwide Distribution: US (nationwide) and countries of: Canada, Argentina, Austria, Australia, Brazil, Chile, China, Colombia, Costa Rica, Germany, Dominican Republic, Spain, France, Great Britain, Hong Kong, Ireland, Israel, India, Korea, Kuwait, Lithuania, Mexico, Netherlands, Portugal, Saudi Arabia, Sweden, Singapore, Taiwan, Venezuela, and South Africa.
BIOMET 3i, PROVIDE PROTECTION CAP KITS, Catalog # PAK4140, PAK4155, PAK4240, PAK4255, PAK4340, PAK4355, PAK4440, PAK4455, PAK5140, PAK5155, PAK5240, PAK5255, PAK5340, PAK5355, PAK5440, PAK5455, PAK6140, PAK6155, PAK6240, PAK6255, PAK6340, PAK6355, PAK6440, and PAK6455     BIOMET 3i Restorative Products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible. Provisional Abutments are intended for use as an accessory to endosseous dental implants to support a prosthetic device in a partially or fully edentulous patient. They are intended for use to support a prosthesis in the mandible or maxilla for up to 180 days during endosseous and gingival healing, and are for non-occlusal loading of provisional restorations.
BIOMET 3i, PROVIDE IMPRESSION COPING KITS,  Catalog # PRK484, PRK485, PRK654, and PRK655    BIOMET 3i Restorative Products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible. Provisional Abutments are intended for use as an accessory to endosseous dental implants to support a prosthetic device in a partially or fully edentulous patient. They are intended for use to support a prosthesis in the mandible or maxilla for up to 180 days during endosseous and gingival healing, and are for non-occlusal loading of provisional restorations.
BIOMET 3i, PROVIDE IMPRESSION COPINGS, Catalog # PIC484, PIC484H, PIC485, PIC485H, PIC654, PIC654H, PIC655, and PIC655H    BIOMET 3i Restorative Products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible. Provisional Abutments are intended for use as an accessory to endosseous dental implants to support a prosthetic device in a partially or fully edentulous patient. They are intended for use to support a prosthesis in the mandible or maxilla for up to 180 days during endosseous and gingival healing, and are for non-occlusal loading of provisional restorations.
BIOMET 3i, PROVIDE PROTECTION CAP, Catalog # PPC484, PPC485, PPC654, and PPC655    BIOMET 3i Restorative Products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible. Provisional Abutments are intended for use as an accessory to endosseous dental implants to support a prosthetic device in a partially or fully edentulous patient. They are intended for use to support a prosthesis in the mandible or maxilla for up to 180 days during endosseous and gingival healing, and are for non-occlusal loading of provisional restorations.
Product was distributed nationwide in the United States.  Foreign distribution to Hong Kong and Mexico.  Product was distributed to military bases in Georgia; no other government distribution.
David Trail Mix Sweet & Salty individual plastic bags net wt. 5 oz. (142 g) UPC 00 26200 23885 2 shipped in the following configurations:    1) cases of eight (8) with UPC 20-0-26200-23885-6;    2) 36-count multi-pack shipper case UPC 00-0-26200-23890-6 which contains 16 individual 5.25 oz. bags of Classic flavor and 20 individual 5 oz. bags Sweet & Salty flavor UPC 00 26200 23885 2; and    3) 24-count snack rack case UPC 27000-82339 store display which contains individual 5 oz. bags Sweet & Salty flavor UPC 00 26200 23885 2.
Distributed to distribution centers and retail stores nationwide.    Distributed to KeHe distribution centers which distribute product to Target stores and WholeFood stores nationwide.  Skinny Latina, LLC directly ships to Fresh Market stores in Florida.
Skinny Latina Million Dollar Marinade, 12 oz, shelf stable, dry storage.
Worldwide Distribution - US (nationwide), Algeria, Armenia, Australia, Austria, Bangladesh, Bosnia Herzegovina, Canada, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Ireland, Italy, Japan, Libya, Malaysia, Poland, Portugal, Romania, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, U.A.E., and United Kingdom.
Siemens Acute Care DDMR TestPak  Catalog Number: CDDMRE  SMN: 10701511    in vitro diagnostic
Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Siemens Acute Care CKMB DilPak- an in vitro diagnostic product intended to be used in conjunction with the Acute Care CKMB TestPak  Catalog Number: CCKMB-D  SMN: 10445070
Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus CS analyzer  Catalog Number: CCCRP-C  SMN:10445067
Siemens Acute Care pBNP TestPak- in vitro diagnostic test for the quantitative measurement of N-terminal pro-brain natriuretic peptide (NTproBNP) in heparinized plasma.   Catalog Number: CPBNPM  SMN: 10445086
MYO TestPak-in vitro diagnostic test for the quantitative measurement of myoglobin in heparinized plasma  Catalog Number: CMYO  SMN:10445079
Siemens Acute Care CKMB TestPak-  in vitro diagnostic test for the measurement of the MB isoenzyme of creatine kinase (ATP: Creatine NPhosphostransferase, E. C. No. 2.7 .3.2) in heparinized plasma  Catalog Number: CCKMB  SMN:10445068
Siemens Acute Care  CTNI TestPak-in vitro diagnostic test for the measurement of cardiac troponin I in heparinized plasma  Catalog Number: CCTNI  SMN: 10445071
Siemens Acute Care MYO DilPak  Catalog Number: CMYO-D  SMN:10445081  in vitro diagnostic
EPSOM SALT(Magnesium Sulfate Heptahydrate, USP), 50 lb multi-wall bag, Rx only, Manufactured by PQ Corporation, P.O. Box 840, Valley Forge, Pennsylvania USA 19482.
Failed Impurities/Degradation Specifications: Level of iron exceeds the limit set by the USP monograph for it (USP limit is NMT 0.5 ug/g (ppm)).
Maquet HCU 30 Coolant Type R134A Filling weight 250 g 120 V 50-60 Hz 1920 W    Product Usage: The Heater Cooler Unit (HCU) 30 is intended to circulate water through heat exchange circuits to warm or cool a patient during short duration cardiopulmonary bypass procedures lasting 6 hours or less.
100 Units (distributed in United States)
Failure of the HEATER-COOLER UNIT (HCU 30) Type 2 power supply board. A drop of more than 10% voltage can cause overheating and subsequent failing of the R56 thermistor of the power supply board. Board failure typically occurs when the compressor is switched on (prior to patient use); however, it can occur during patient use. This can shut down the compressor or the entire HCU 30 Type 2 unit.
HCU 30 Base Unit 100 - 120 V, Model Number 704629/70103.4371  HCU 30 Base Unit 200 - 240 V, Model Number 704631/70103.4642  HCU 30 Base Unit Canadian/US, Model Number 705501/70103.4653  Heater Cooler Unit 30 with Serial Number <93101480    The affected power supply boards have serial numbers less than 107006001.
Casey's Bakery, 8X8 Snickers cake, www.caseysbakery.com, Sioux Center, IA
Made In Nature Sriracha Chili Kale Chips, 2.2oz or 62g, In a clamshell container with a paper sleeve,  8 packages per case
Made in Nature is recalling Made In Nature Sriracha Chili Kale Chips and Pacific Superfoods Snack Lava Rock Sriracha Kale Chips due to undeclared soy allergen from Tamari.
Pacific Superfoods Snack Lava Rock Sriracha Kale Chips, 2.2oz or 62g, In a clamshell container with a paper sleeve,  8 packages per case
Device has the potential to have torn wings.
Model No.: FS+173230BC, Lot #14A22 and Lot #14A26.
Nationwide Distribution including MI and CA.
CNSystems TASK FORCE MONITOR 3040i, plethysmograph, impedance.  Noninvasively measure and display patient's hemodynamic parameters time synchronized using Impedance Cardiography (ICG), Electrocardiography (ECG), oscillometric Blood Pressure (oscBP) and continuous Blood Pressure (contBP). Furthermore Sympathic Tone and Parasympathic Tone are calculated by power spectral analysis of ECG (heart rate variability) and continuous blood pressure (blood pressure variability) as well as the Baroreceptor Reflex Sensitivity (BRRS). For use by medically trained personnel. It has been designed for diagnoses aiding and must not be used for vital sign monitoring of critically ill patients under absence of additional, suitable self-monitoring devices or medical trained personnel. The device measures continuously the subject's hemodynamic parameters without reporting any diagnosis. It is the physician's responsibility to make proper judgment based on these parameters.
28 worldwide 2 monitors distributed in the U.S.
Device non-conformity which may lead to an incorrect oscillometric measurement of upper arm blood pressure values in some subjects - mainly in tall and slim persons (overestimation of systolic blood pressure, underestimation of diastolic blood pressure).
US Distribution in the states of: AK, CA, WI, IN, FL, OR, NY, and NC.
The Fuhrman Pleural/Pneumopericardial Drainage Set    The Fuhrman Pleural/Pneumopericardial Drainage Set consists of pigtail catheter, access needle, dilator, and wire guide. The set also includes a multipurpose tubing adapter, and three-way stopcock.
Stryker Sustainability Solutions is recalling the Fuhrman Pleural & Pneumopericardial Drainage Set due to receiving complaints that it broke off in the pleural cavity while inserting the device into the patient.
Worldwide distribution.  US nationwide, France, UAE, Austria, Australia, Belgium,  CANADA, Switzerland, Germany, Denmark, Spain, Finland, UK, Hong Kong, ISRAEL, India, Italy, Japan, South Korea, Netherlands, Norway, Poland, PORTUGAL, Sweden, SINGAPORE, Thailand, Turkey, and SOUTH AFRICA.
BIRMINGHAM HIP RESURFACING MODULAR HEAD, REF numbers:    74121238, MODULAR HEAD 38 MM -8MM  74121242,  MODULAR HEAD 42 MM -8MM  74121246,  MODULAR HEAD 46 MM -8MM  74121250,  MODULAR HEAD 50 MM -8MM  74121254,  MODULAR HEAD 54 MM -8MM  74121258,  MODULAR HEAD 58 MM -8MM  74121338,  MODULAR HEAD 3 8MM -4 (SHORT)  74121342,  MODULAR HEAD 42 MM -4 (SHORT)  74121346,  MODULAR HEAD 46 MM -4 (SHORT)  74121350,  MODULAR HEAD 50 MM -4 (SHORT)  74121354,  MODULAR HEAD 54 MM -4 (SHORT)  74121358,  MODULAR HEAD 58 MM -4 (SHORT)  74121438,  MODULAR HEAD 38 MM +0 (MED)  74121442,  MODULAR HEAD 42 MM +0 (MED)  74121446,  MODULAR HEAD 46 MM +0 (MED)  74121450,  MODULAR HEAD 50 MM +0 (MED)  74121454,  MODULAR HEAD 54 MM +0 (MED)  74121458,  MODULAR HEAD 58 MM +0 (MED)  74121538,  MODULAR HEAD 38 MM +4 (LONG)  74121542,  MODULAR HEAD 42 MM +4 (LONG)  74121546,  MODULAR HEAD 46 MM +4 (LONG)  74121550,  MODULAR HEAD 50 MM +4 (LONG)  74121554,  MODULAR HEAD 54 MM +4 (LONG)  74121558,  MODULAR HEAD 58 MM +4 (LONG)
The 16 devices distributed in the United States were incorrectly labeled as the monoblock Birmingham Hip Modular Head, with labeling not cleared for marketing in the US.  The actual devices were monoblock Modular Femoral Head for hemiarthroplasty use.
Worldwide Distribution - US (nationwide) and Internationally to Canada , Taiwan , Singapore , and England.
HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE  Model : 75-7500-038  Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
Knee  brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,
(1) all braces that begin with a Revision Code of AN, AP, AQ, AR, AS, AT, AU are to be returned to Corflex immediately for review; (2) all braces with a Revision Code beginning with AM and that comply with the date range:  Braces manufactured between September 1, 2015 and November 6, 2015
Corflex Contender Post-Op Knee Brace Lite  Model: 75-7500-000  Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE  Model: 75-7500-087    Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE  Model: 75-7500-231  Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE	  Model: 75-7500-011    Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.  Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE  Model: 75-7500-075  Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
CONTENDER POST-OP-KNEE BRACE FULL FOAM  Model: 75-7550-000  Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
Oklahoma Blood Institute - Sylvan N Goldman Center
Apheresis Red Blood Cells, Leukocytes Reduced
Leukoreduced blood products, not tested for residual WBC count, were distributed.
Worldwide Distribution - US (nationwide) and Internationally to Argentina, Australia, Austria, Belgium, Colombia, Cyprus, Czech Republic, Egypt, Finland, France, Germany, Great Britain, Greece, Hong Kong, Ireland, Italy, Japan, Malaysia, Netherlands, Poland, Portugal, Serbia, Singapore, Slovenia, Spain, Sweden, Switzerland, and Thailand.
Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter, 9 Fr.  Model 8104, 8105, 8106, 8107, 8108, 8109, 8110, 8111, 8112, 8113, 8114, 8115, 8116, 8117, 8118, and 8119.      The ACUITY Pro Lead Delivery System is designed for venous use to aid in the selective placement of cardiac resynchronization therapy (CRT) implantable venous leads in the cardiac vasculature.  The catheter shafts are comprised of a PTFE inner liner, a reinforcing layer of stainless steel braid, and an outer polymer jacket.  The distal end has a radiopaque polymer tip, while the proximal end has a hub with flush luer fitting to allow flush, contrast injection and aspiration polymer .
Potential for separation of the proximal handle from the shaft.
Worldwide Distribution to Germany, Belgium, Denmark, France, UK, Greece, Ireland, Netherlands, Norway, Russian Fed., Saudi Arabia, Sweden, and Thailand.
NexGEN System REF 5980-37-01 Tibial Component  Size Stemmed 3 Precoat, and REF 5986-37-01 Nonaugmentable Tibial Component  Option CR/PS/LPS Size Stemmed 3.   Tibial component of implanted knee prosthesis.
384 distribution events; 1 unit was returned leaving 383 units  .
A product complaint was received stating that a carton labeled as a Precoat Stemmed Tibia Size 3 was opened for use and the contents were a non-augmented Stemmed Tibia Plate size 3.
Nationwide Distribution including:  AL, AZ, CA, CO, FL, IA, ID, IL, IN, MA, MD, MI, MN, MO, MT, NC, NY, OH, OK, PA, SC, TN, TX, VA, and WI.
Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.
on X-Workplace with software version VD10E. A too small measurement in the MPRs of a volume when images are acquired with a CT scanner with a tilted gantry. In a 2x2 layout, the 4D tabcard will show an incorrect, too small length measurement. This could result in selecting a device of the wrong size, which then needs to be exchanged.
ActiV.A.C. 300ml Canister (with Gel) for ActiV.A.C. Therapy System for the application of V.A.C. Therapy in the acute extended and home care settings. The software-controlled therapy unit applies negative pressure wound therapy. The dressing, to which the therapy unit is connected, enables distribution of the negative pressure across the surface of the wound, while the tubing transfers accumulated fluids to the canister.
There is potential for small holes, the size of a pin, to develop in the pouches of the ActiV.A.C. Sterile Canisters.
Models M8275058-JP/5 and M8275059/5.  manufactured between October 5, 2014 and May 29, 2015.  Labeled with a 23 month shelf life from the date of manufacture.
Natus Neurology DBA Excel Tech., Ltd. (XLTEK)
Worldwide Distribution: US Distribution including states of: AL, AZ, AR, CO, FL, GA, MD, MA, MN, MS, NJ, NY, OH, SC, TN, TX and UT; and countries of: INDIA, KOREA, SPAIN, SWITZERLAND, THAILAND, UNITED KINGDOM, and CANADA.    .
Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926.    The Natus Quantum Amplifier is intended to be used as an electroencephalograph: to acquire, display, store and archive electrophysiological signals. The amplifier should be used in conjunction with Natus NeuroWorks /SleepWorks software to acquire scalp and intracranial electroencephalographic (EEG) signals as well as polysomnographic (PSG) signals.
During an internal testing, Natus Medical Incorporated, identified that in Neuro Works 8.1 with Quantum hardware, the incoming signal is displayed with reversed polarity.
Blood products, possibly contaminated with air, were distributed.
Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed
Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
SYNTHES; 13.5MM Medullary Reamer Head; 352.135 NON STERILE. Part of the Flexible Reamer Set for orthopedic surgical procedures.
The 13.5mm Medullary Reamer head, lot #F-17180, is etched as dimension 13.5mm while the actual dimension is 14mm.
Part number: 352.135;   Lot number: F-17180
3m Center 2510 Conway Ave , B# 275-5-W-6
3M Coban Self-Adherent Wrap Shipper carton label identified the product as 3M Coban LF Latex Free Catalog #2081, lot number 2018-10AM.
Product mislabeled as latex free.  Actual Catalog number 1581, lot 2020-10AN. contains latex. This could pose a health risk to  users with sensitivity or allergic reaction to latex, which could range from mild to severe.
Catalog# 1581, lot # 2020-10AN  Catalog# 2081, lot # 2018-AM (shipper carton)
Blood product, collected from a donor who traveled to a malarial endemic area, was distributed.
US Nationwide Distribution and the country of Canada
Potential for dark loose particulate matter (400 microns or smaller) on the spike of the spike adapter or solution set.
Baxter CLEARLINK System, Blood Bag Spike Adapter, Luer Activated Valve for I.C. Access, 1C8687,     Product Usage:  C8687: An accessory to transfer a medicinal product from one container to another container.
US Nationwide distribution in the states of  AZ, CA, MD, NM, NJ, and OH.
Remote Patient Monitoring System, MDP 2000 Series, Part Numbers: MDP2040-0100, PGM340R3, or PGM340R4.    The MDP2000 is intended for use in conjunction with patient monitoring equipment. The MDP2000 is not patient connected Examples of areas where the MDP200 is used include ICU, CCU, PACU, Emergency, Telemetry Step-down and other areas where patient's physiological information are to be observed at one or more locations. Typical information displayed includes ECG and blood pressure waveforms and numeric values which as heart rate and systolic, mean and diastolic pressure. This device acts as the Central Monitor Station, it permits from one (1) to sixteen (16) bedside monitor(s) to be connected simultaneously.
Testing at customer site showed unit Remote Patient Monitoring System MDP2040-0100 in a continuous trap condition, not allowing system to reset and reboot.  Two customers recently complained of the system freezing and it could only be restarted if the user re-applied power.
(a) 2 containers, (b) 32 containers, (c) 48 containers
Product was shipped to the following states: AL, GA, ID, IL, IN, KY, LA, MI, MO, MT, NM, NV, OH, SC, TN, TX, UT, WV & WY.
BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS: MILK, EGGS, WHEAT, SOY. MAY CONTAIN: ALMONDS, PECANS, WALNUTS, CASHEWS, COCONUT. DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 UPC 0 11110 09172 7
The firm was notified by a consumer of undeclared walnuts in the product.
American National Red Cross, Penn Jersey Region
Blood and Blood Products for Reprocessing
Blood products, collected from donor for whom donor suitability was not adequately dertermined, were distributed.
Worldwide Distribution - US Nationwide and the countries of Austria, Canada, Colombia, Denmark, France, Germany, Great Britain, Iceland, and Portugal.
InterGuard 5.5mm Econo Refill, sizes, 4.0mm for short anatomical crowns and 5.5mm, part # 4012    Product Usage:    InterGuard is a preventive aid for operative dentistry. It is used to protect adjacent teeth from iatrogenic preparation damage. This includes cavity and tunnel preparations as well as air abrasion.
Ultradent is recalling InterGuard 5.5mm Econo Refill, lot#s BC2GN and BC4L7 because product was received from the supplier with the floss tether hole not completely punched through and were distributed.
Distributed in the US including: CA, IL & NC; Canada
Magnesium Sulfate 7-Hydrate, (For Parenteral Use) USP -GenAR, 100LB, Avantor Performance Materials, Inc., 3472 Corporate Parkway, Suite 200 Center Valley, PA 18034. 610-573-2600.
Failed Impurities/Degradation Specifications: Out of specifications results for impurities.
Worldwide Distribution: US (nationwide) and countries of: Australia, Austria, Bahrain, Canada, China, Colombia, Costa Rica, France, Hong Kong, India, Indonesia, Israel, Kuwait, Lebanon, Mexico, Panama, Peru, Republic of Korea, Russian Federation, Saudi Arabia, Singapore, Spain, Taiwan, Thailand, Turkey, Uganda, United Arab Emirates, Viet Nam & Virgin Islands.
The firm discovered that information printed on the quick reference magnet is incorrect; specifically, Fahrenheit to Celsius temperature conversions and the default Warming Cabinet temperature.
Nicomex Velitas Candies Candles Net. Wt. 2 oz (56.7 gms) Distributed by Nicomex Inc. 88 First Street, Passaic, NJ 07055
This recall has been initiated because the laboratory analysis indicates that the product contains FD & C Red #3, and Yellow #5 which are not declared on the ingredient statement on the product label.
Crazy about Cookies 2lb DSC Custom Decorated Sugar Cookies Item # 101-2207 thru 101- 2355  UPC Code - None
Pre-portioned sugar cookie dough contains undeclared milk and pre-portioned walnut chocolate chunk cookie dough contains undeclared egg.
Crazy about Cookies 2lb Fairytale Princess COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4031 UPC Code - 698768034315
Crazy about Cookies 2lb Monster Bash COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4032 UPC Code - 698768034322
Crazy about Cookies 2lb Holiday Gathering COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4034 UPC Code - 698768034346
Crazy about Cookies 2.7lb Sugar Cookies Pre-Portion Item # 25-2004 UPC Code  - 698768102120
Crazy about Cookies 2lb Birthday Celebration COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4033 UPC Code - 698768034339
Crazy about Cookies 2lb HELLO KITTY COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4035 UPC Code - 698768034353
Crazy about Cookies 2.7lb WALNUT CHUNKY CHOCOLATE CHIP Pre-Portioned cookie dough Item # 25-2008 UPC Code - 698768102168
Worldwide Distribution: US (nationwide) including Puerto Rico and countries of: India, Belgium, Argentina, Mexico, Brazil, Canada, Colombia, Ecuador, Singapore, Aruba and Venezuela.
Stability data does not substantiate the labeled two-year shelf life of affected product.
Blood product, which was collected from a donor who lived in a malarial endemic area, was distributed.
Worldwide Distribution - US including GA & Internationally to Canada.
(91CM) Polyurethane Feeding Tube For Pediatric Use with Orange Radiopaque Stripe and Enteral Connector, Made in Canada, Benton, Oakville, Ontario, Canada
The product may be packaged with a 5 or 6.5FR tube instead of an 8FR size.
US Distribution to states of:FL, MO, IN and TX.
Smith & Nephew GENESIS(R) II/LEGION(TM)  PATELLAR COMPONENT, RESURFACING ROUND, 32MM STANDARD, FOR CEMENTED USE ONLY WITH JOURNEY PEG, STERILE EO, Rx only, REF Number: 71934490    knee implant.
One lot of 35 mm patella implants is labeled as 32 mm.  These implants have pegs which are spaced proportionally; therefore the mismatch prevents the pegs from properly aligning with pre-drilled holes during implantation.
Worldwide Distribution - US Nationwide in the states of CA, NY, PA, and the countries of  Austria, Belarus, Canada, China, Denmark, Finland, France, Germany, Greece, India, Italy, Japan, Netherlands, Norway, Poland, South Korea, Spain, Sweden and United Kingdom.
Oncentra External Beam - VMAT - Radiation therapy planning system    Product Usage:  The Oncentra system is a radiation treatment planning software designed to analyze and plan radiation treatments in three dimensions for the purpose of treating patients with cancer.
in VMAT planning it has been observed that in rare cases the system does include an organ at risk as target volume.  This could result in open MLC, and open jaws in areas away from the target volume.
distributed in CA, CT, ND, NV, OR, RI, TN, and WA.
Philips Lumify Diagnostic Ultrasound, Catalogue Number: 795216  Part Number: 989605449841 with 453561845331 (software version 1.0)
Color Flow direction is displayed incorrectly in Lumify 1.0. The system displayed Color Flow direction does not correctly represent the annotated Color Bar or Velocity Markers. (e.g.) When the Color Bar conveys that Red is to be displayed for color flow toward the Transducer, the system displays Blue for color flow toward the Transducer. This could result in misdiagnosis in some studies.
The American National Red Cross - Southern Region
Blood products, collected from a donor for whom donor suitability was not adequately determined, were distributed
Apheresis products for which pH testing was not performed, were distributed.
Apheresis Platelets, Leukocytes Reduced, Irradiated
Apheresis product, with a low platelet yield, was distributed.
Azithromycin Tablets, USP, 250 mg, Rx Only, packaged in a) 2 count and b) 4 count bottles, Packaged by: PD-RX Pharmaceuticals, Inc., Oklahoma City, OK, 73127, Mfg: Wockhardt Ltd., Mumbai, India, NDC: a) 55289-964-02, b) 55289-964-04.
cGMP Deviations: This recall is a result of the original manufacturer's recall, in which the firm did not adequately investigate customer complaints.
Azithromycin 500 mg tablets, Rx Only, packaged in a) 1 count, b) 2 count, c) 3 count, and d) 7 count bottles, Packaged by: PD-RX Pharmaceuticals, Inc., Oklahoma City, OK 73127, Mfr: Wokhardt Ltd., Mumbai, India, NDC: a) 55289-274-79, b) 55289-274-02, c) 55289-274-03, d) 55289-274-07.
Ottobock Modular Polycentric EBS Knee Joint 3R60, 3R60=ST, 3R60=KD, 3R60=HD.  Used for the prosthetic fitting of amputations of the lower. limb.
Otto Bock HealthCare GmbH is recalling Modular Polycentric EBS Knee Joint that were serviced between 27 April 2015 and 17 November 2015 due to a service error where the wrong Loctite was  used during repair.
All serviced between 27 April 2015 and 17 November 2015