Product was distributed to wholesalers in KS, MO, and OH.  There was no foreign/military/government distribution.
GentaVed Topical Spray.  For Animal Use Only. ANADA 200-416. Each mL contains: gentamicin sulfate, USP equivalent to 0.57 mg gentamicin base, betamethasone valerate, USP equivalent to 0.284 mg betamethasone.  12-60 mL bottles/carton, Sparhawk Laboratories, Inc., Lenexa, KS 66215-3591.
Betamethasone Valerate in recalled product found below specification at the 18 month stability time point.
AR, CA, CO, DE, FL, GA, IL, MN, NJ, NC, OH, OR, PA, SC, TN, TX,VA, WI, Santa Domingo, & Guam
BM Westco Mster Mix Raised Donut Mix, 50#
CA, ID, MN, NY, PA, SD, TX, WI.  No international.
Syringes appear to be more brittle than the previous syringes, which may result in cracks in the barrel of the syringe.  A cracked syringe barrel has the potential to impact the sterility of the product. Considering the indications of the product, it is assessed that the involved batch of the product has the potential to pose a microbial risk in the target animals. If there is a contamination, possible injection site abscess may result. If the infection spreads from local site, fever or upper respiratory or gastro intestinal infections could occur.
Batch C554686  expiration date of Oct 2019
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Nationwide and foreign.  No VA/govt/military consignees.
Protein Chews Raspberry,1.8oz, film package, 12 packets per box.
EN-R-G Foods is recalling Cherry Lime Protein Chews, Raspberry Protein Chews, Juneberry Protein Chews due to complaints of nausea and/ or vomiting after consumption.
Protein Chews Juneberry,1.8oz, film package, 12 packets per box.
Protein Chews Cherry Lime,1.8oz, film package, 12 packets per box.
Distributed throughout the US, Canada, and New Zealand.
Metrix Donor Set W/15 Gauge Needle, Part # 3080, non-sterile, not for human use, packed in 25 per polybag, 400 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
The hub of the needle on affected products may contain aluminum flakes.
Metrix Donor Goat Set, Part # 3120, non-sterile, not for human use, packed in 25 per polybag, 200 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Lot numbers: 3120-27940 (Lot 3120-28392 was scrapped by the firm)
Metrix Bleeding Bag 12G Inner Seal, Part # 4630, non-sterile, not for human use, packed in 150 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Metrix 2L Blood Donor Bag with Needle, Part # 7310, non-sterile, not for human use, packed individually in polybags, 100 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Metrix 600ML Blood Donor Bag, Part # 7070, non-sterile, not for human use, packed individually in polybags, 125 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Metrix Bleeding Bag, Part # 2150, non-sterile, not for human use, packed in 200 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Metrix 1L Defibro Bag, Part # 4770, non-sterile, not for human use, packed in 60 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Lot numbers: 4770-A1719   (Lots 4770-A1720, 4770-A1721, and 4770-A1722 are quarantined at the firm)
Metrix 12Gauge Donor Set, Part # 5350, non-sterile, not for human use, packed in 25 per polybag, 200 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Metrix Bleeding Bag 15 G Needle, Part # 2000, non-sterile, not for human use, packed in 200 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Metrix 1L Defibro Bag, Part # 2560, non-sterile, not for human use, packed in 60 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Metrix Bleeding Bag 15G Needle, Part # 2210, non-sterile, not for human use, packed in 200 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002.
Enlightened Peanut Butter Chocolate Chip Ice Cream, one pint
Select cases from a single production run of Enlightened brand Peanut Butter Chocolate Chip ice cream is being recalled because they may have been packaged in Mint Chocolate Chip ice cream containers and thus contain undeclared peanuts.
Distributed to NE, OR, KS, PA, IA, MO, OH, IL, TX, IN, UT, TN, NY, FL, VA, and Puerta Rico.
Organic Cacao Nibs, packaged in 200g (7.05 oz) brown bags,  UPC code 661594002032
480kg packaged into 2400 packages of 200g each
Lot numbers: 241201 and 641102.  Both are best by April 2017
Merit Medical Systems, Inc. announces a voluntary field action for Fluid Administration Sets due to mold in the drip chamber.
4% cottage cheese packaged in 16-ounce, 22-ounce, and 24-ounce plastic containers; under the Westby, Food Club, Oberweis, and Shurfine brand names.
The firm is conducting a recall of the 4% cottage cheese because the product tested positive for residue phosphatase.
Greatbatch Stiffer Coaxial Micro-Introducer. Model #/ Name: 10904-001 Stiffer Coaxial Micro-Introducer 4FR; 10904-002 Stiffer Coaxial Micro-Introducer 5FR.    The radiopaque Stiffer Coaxial Micro-Introducer (Figure 1) consists of a dilator and sheath, available in 4FR and 5FR. The inner dilator includes a stainless steel stiffening hypotube. The Coaxial Micro-Introducer is indicated for percutaneous introduction of up to a 0.038 in. guidewire or catheter into the vascular system through an initial puncture of a 21G introducer. The device is sold to customers  in a bulk non-sterile configuration.
Greatbatch Medical has identified an issue with the Stiffer Coaxial Micro-Introducer 4FR and 5FR after a field complaint reported that the rotating luer detached from the dilator hub during use.
Phenobarbital Tablets, USP 60mg 100=count bottles, Rx Only, Mfd. by: West-Ward Pharmaceutical Corp. Eatontown, NJ 07724, NDC 0143-1455-01
Failed Dissolution Specifications: Phenobarbital Tablets have an out of specification for dissolution at the 12 month stability time point
Nationwide Distribution including AL, CA, FL,IN, MI, MO, NY, PA, TN, and WI.
It was reported by a customer  that RadSuite images are not appearing as readable images.     This product malfunction has the potential to result in delay in care and a possible re-exposure of the patient to radiation (x-ray).
Domestic: Alabama, Illinois, Kansas, Massachusetts, Mississippi, Missouri, Ohio, Vermont.
12ct Banana Nut mini muffins labeled as 12ct Lemon poppy seed mini muffins; Date code 160803 ink jet printed on top near the label.
1170 cases of Banana nut mini muffins labeled as Lemon poppy seed mini muffins
Pentax Video Colonoscope is intended to be used with a PENTAX video processor (including light source), documentation equipment, Monitor, EndoTherapy Device such as a Biopsy Forceps, and other ancillary equipment for endoscopy and endoscopic surgery within the lower digestive tract including the anus, rectum, sigmoid colon, colon and ileocecal valve.
Pentax is initiating the product correction of several model numbers of Pentax's Colonoscope that were shipped between the clearance date of April 2014 and September 2015 because they contain the operation and reprocessing IFU's that were in use prior to the 2014 clearances and therefore did not include the cleared operation IFU, the updated reprocessing IFU or the dedicated reprocessing adaptor (for applicable models).
Worldwide Distribution-U.S. Nationwide and country of: Canada.
PeroxiClear Peroxide Solution, (3oz. and 12 oz., 12 oz. Twin Pack, 2x12 oz. Twin Pack for Target stores, 12 oz. for Walmart Vision Center and 3 oz. Starter Kit US), Manufactured by Bausch + Lomb, Rochester, NY 14609.    PeroxiClear 3% Hydrogen Peroxide Cleaning & Disinfecting Solution is indicated for the daily cleaning, removal of protein deposits, disinfection and storage of soft (hydrophilic) contact lenses (including silicone hydrogel) and rigid gas permeable contact lenses.
Product was found to contain excess residual levels of hydrogen peroxide.
Item #623815, UPC: 310119038154, Lot number: GE15012ST, Lot Exp. Date: 2016/11/30, Lot number: GF15055ST, Lot Exp. Date: 2016/12/31, Lot numbers: GH15053R, GH15056-1, GH15067ST, GH15070ST, GH15076ST, GH15081ST and   GH15086-1, Lot Exp. Date: 2017/02/28, Lot numbers: GK15116ST, GK15118A1, Lot Exp. Date: 2017/04/30, Lot numbers: GL15148-1 and GL15148-2, Lot Exp. Date: 2017/05/31, Lot number: GC16080-1, Lot Exp. Date: 2017/09/30 and 623815C (3 oz.), Lot numbers: GE16060A1 and GE16066-1, Lot Exp. Date: 2017/11/30; Item #623816 (12oz.), UPC 310119038161, Lot numbers: GC15002ST, GC15008ST, GC15008ST1 and GC15012AST, Lot Exp Date: 2016/09/30, Lot numbers: GD15100ST1, GD15115AST, GD15124ST and GD15124ST2, Lot Exp Date: 2016/10/31, Lot numbers: GE15132ST and GE15156ST, Lot Exp Date: 2016/11/30, Lot numbers: GF15110ST and GF15110ST1, Lot Exp Date: 2016/12/31, Lot numbers: GG15023STR, GG15038ST and GG15044ST, Lot Exp Date: 2017/01/31, Lot numbers: GH15036ST, GH15039ST, GH15045ST and GH15128ST, Lot Exp Date: 2017/02/28, Lot numbers: GJ15070ST and GJ15081ST, Lot Exp Date: 2017/03/31, Lot numbers: GK15129ST and GK15131ST, Lot Exp Date: GL15004STR, GL15012ST and GL15048ST, Lot Exp Date: 2017/05/31, Lot numbers: GM15027AST, GM15034ST, GM15041ST and GM15044ST, Lot Exp Date: 2017/06/30, Lot numbers: GA16023ST1, GA16052ST and GA16056ST, Lot Exp Date: 2017/07/31, Lot numbers: GC16035ST, GC16044ST and GC16060ST, Lot Exp Date: 2017/09/30, Lot numbers: GE16001ST, GE16004ST, GE16009ST and GE16009ST1, Lot Exp Date: 2017/11/30, Lot numbers: GF16087ST and GF16087ST1, Lot Exp Date: 2017/12/31, Lot number: GG16003ST, Lot Exp Date: 2018/01/31 and 623816B, UPC 310119038161, Lot number:  GG16116ST, Lot Exp Date: 2017/10/31; Item #623817 (12 oz. Twin Pack), UPC 310119038178, Lot number: GC15026ST, Lot Exp Date: 2016/09/30, Lot numbers: GD15095ST, Lot Exp Date: 2016/10/31, Lot numbers: GE15131ST, GE15133ST, GE15149ST and GE15161AST, Lot Exp Date: 2016/11/30, Lot number: GF15107ST1, Lot Exp Date: 2016/12/31, Lot numbers: GG15002STR and GG15037
Nationwide and Canada. No other foreign and military/govt/VA consignees.
Original HCG. 2oz HCG Drops. Amber Glass
The firm announced a voluntary recall of various dietary supplement products due to misbranding and some products may contain undeclared HCG.
A New You HCG. 1oz HCG Drops. Blue Glass.
Slimming Herbs. 2oz HCG Drops. Amber Glass
Simeons Program. 2oz HCG Drops. Amber Plastic.
Amino Complex Formula. 2oz HCG Drops. Blue Glass.
Natural Protocols. 2oz HCG Drops. Amber Glass
Pounds and Inches. 1oz HCG Drops. Amber Glass.
Health & Beyond. 2oz HCG Drops. Amber Glass.
Athens Clinic of Clinic of Chiropractic. 2oz HCG Drops. Blue Glass.
Omni Drops. 4oz HCG Drops. Amber Plastic
B-Slim. 2oz & 4oz HCG Drops. Blue Plastic.
Supervision Weightloss. 2oz HCG Drops. Amber Glass
HCG Complex. 2oz HCG Drops. Blue Plastic.
Official HCG Diet Plan. 1oz, 2oz & 4oz HCG Drops. Amber Plastic and Glass.
Nationwide to VA, UT, and NC. Other foreign consignee Japan. No Canadian and VA/govt/military consignees.
Manifold Kit. Catalog Number K09-11867AP
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Waste Management Kit. Catalog Number K10-04381AP
Fluid Management Set. Catalog Number K08-MP5159A
Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A
Worldwide Distribution -- USA, in the following states AL, AR, AZ, CA, CO, CT, GA, FL, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, WA, WI, & VA; and, to the countries of Albania, Australia, Belgium, France,  Germany, Ireland, Italy, Norway, Netherlands, Poland, Sweden, Turkey, United Arab Emirates, & United Kingdom.
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System.  Model Numbers: 700-001, 700-001S, 700-001MI, 700-002, and 700-003.    Intended to ablate cardiac tissue during cardiac surgery using radiofrequency (RF) energy when connected directly to the Estech Electrosurgical unit (ESU).
Due to product design and process control, part of the device can separate and remain behind when the device is removed that can potentially cause permanent impairment or damage to body function or structure.
on the product label as: MM-YYYY, e.g. 02-2016 or earlier.
Product was distributed to NE, OK, KS, MO, AZ, and TX.
Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
Product may be contaminated with Listeria Monocytogenes.
Distributed to the following states: AL, FL, GA, NC, SC, & TN.
Publix Premium Chocolate Cookie Dough Ice Cream, 1/2 gallon carton.
Possible contamination with Listeria monocytogenes.
NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and distributed by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-2407-10
US Distribution to states of: CA, ID, IL, IN, KS, KY, LA, MO, NC, OR, PA, TX, VA, WA, and WV.
SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.
Lot Codes:  AMMBPW  AMPCML  ANCDJ0  APPBYD
Yoma Myanmar Tea Salad Snack - Regular, 7 oz cello bag. Product of Myanmar
Yoma Myanmar Tea Salad Snack - Spicy, 7 oz cello bag. Product of Myanmar
AHP NIFEdipine Capsules, 10mg USP, 100 count carton (NDC: 68084-022-01); Individual Blister (NDC: 68084-022-11), Rx Only, Manufactured by: Actavis Elizabeth, LLC, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217
5283 cartons (100 capsules per carton = 528,300 capsules)
USA (nationwide)  Distribution and Worldwide Distribution including the states of :  AR, AZ, CA, FL, ID, NJ, NV, NY and PA.., and to the countries of :   Saudi Arabia, Colombia, Mauritius, Iraq, Mongolia, Greece, Albania, Austria, Bosnia, Bosnia Herzegovina, Belarus, Bulgaria, Macedonia, Poland, Serbia, Dominican Rep., Tunisia, Paraguay, Hungary, Jordan, Egypt, Belgium, Caribbean, Germany, Brazil, Mexico, Italy, India, South Korea, Cyprus, Bangladesh, Morocco, Chile, Bahrain, Palestine, Utd.Arab.Emir., Kosovo, Uruguay, Venezuela, Hungary, Australia, Vietnam, Sri Lanka, Turkey, Vietnam, Romania, Mauritius, Ecuador, Lebanon, Nepal, Argentina, Hong Kong, China and Canada.
LIAISON Estradiol II Gen, 310680, 310680-CN    The DiaSorin LIAISON Estradiol II Gen assay is a chemiluminescent immunoassay (CLIA) intended for the quantitative determination of estradiol in human serum. Assay results should be used in conjunction with other clinical and laboratory data to assist in the diagnosis and management of conditions involving an excess or deficiency of estradiol. The test has to be performed on the LIAISON Analyzer Family.
Worldwide Distribution - US (Nationwide) Internationally to  Australia, Austria, Bahamas, Belgium, Canada, Czech Republic, Denmark, Finland, France, Germany, Great Britain, Italy, Japan, Netherlands, New Zealand, Norway, Portugal, Qatar, Saudi Arabia, South Korea, Slovakia, Slovenia, Spain, and Switzerland.
Device Listing Number: D011448 (Kc110) and D244577 (KC110B)  Lot numbers: MGM081 and MGM082
HEARTLAND ENTREES DUMPLINGS AND BROTH, Product Code 856140, NET WEIGHT:  (320 ozs)(9.09 kg)(4-5 Lbs), KEEP FROZEN
Dumplings in the Broth and Dumplings product contains undeclared milk.
PRODUCTION DATE 9/13/16, CODE DATE 15627
2.5 mm TI Calibrated Reaming Rod 850 mm, Sterile
The peel pouches for the affected reaming rods and extraction hooks are delaminating.
Extraction Hook - Sterile for TI Cannulated Nails
Catalog ID 355.399S, Lot Numbers: H102610
3.0 mm Reaming Rod/950 mm w/straight Ball Tip, Sterile
2.5 mm Reaming Rod W/Ball Tip 650 mm, Sterile
2.5 mm Reaming Rod with Ball Tip & Extension/950 mm, Sterile
3.0 mm Guide Rod/950 mm with Smooth Tip, sterile
2.5 mm Guide Rod w/Smooth Tip 950 mm, Sterile
Worldwide Distribution - US Nationwide and the countries of Belgium, Botswana, Canada, Chile, Columbia, Czech Republic, Denmark, Finland, France, Germany, Ghana, Italy, Malaysia, Netherlands, Poland, Romania, Slovakia, South Africa, Spain, Sweden, Switzerland, United Kingdom and Zambia
AQUIOS Lyse Reagent Kit, Catalog No. B23538    Product Usage:  AQUIOS Lysing Reagent Kit is used as part of the AQUIOS flow cytometer system. The kit consists of two reagents used by AQUIOS flow cytometers to prepare whole blood samples for analysis of white blood cells.
Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead to an increased generation of notifications and flags when used on the AQUIOS CL when running the AQUIOS Tetra application.  The issue could lead to an increase in the number of samples requiring review and re-runs with a potential delay to the reporting of results. Depending on the specimen age, a new blood specimen may be required.
US Distribution to the states of : AL, FL, ID and MA.
Pathfast D-Dimer, Reference number: PF1051-KUS
42 boxes (each containing 60 test cartridges/one kit contains 10 reagent cartridge trays and one tray has 6 cartridges).
Two complaints were received about decrease in sensitivity (control value and/or calibration value) of the product.
Product was distributed in the following states: IL, MI, and OH.
Three Way Popcorn Sampler that contains three types of popcorn (cheese, carmel and buttered popcorn) packed inside one unlabeled clear plastic bag, physically divided by a three-way paperboard divider.  The bag is packed inside a metal tin.
Undeclared eggs on the finished product label.
US Distribution to the states of: CA, KY, LA, MD, ME, NC, NH, NY, TX, VA, WA    Foreign: Austria, Ireland, and Japan    VA/DOD:
ACTIS Flex Reamers SZ 0/1; 2/3; 4/5; 6/7; 8/9; 10/11; 12, Product is sold non-sterile, these instruments are packed non-sterile, within a rigid tube with foam protectors, with label and IFU
DePuy Orthopaedics, Inc. is issuing a voluntary recall for all lots of the ACTIS Flex Reamers due to the instruments breaking and potentially leaving pieces in the patient.
Stewart's SPORTADE FRUIT PUNCH Isotonic Beverage 20 Fl Oz (591 mL), UPC 0 82086 31006 8. The product is packaged in a plastic bottle, and has a black label with a red plastic cap.
The specific code of SPORTADE FRUIT PUNCH may contain undeclared milk.
Expiration date code DEC 02 (found on the neck of the bottle)
Philips Electronics North  America Corporation
USA(nationwide) Distribution to the states of : AZ, NY, GA, UT, TN, TX, AR, NV, Il, FL, MS, LA, MD, MO, MA, OK, KY, WY, SC, ND, NE, DE, MI, WA, CT, RI, KS, OR, IN, PA, CA, NJ, NC, MN, AL and IA.
Philips Healthcare System X-ray Tomography Computed :
It was discovered the patient support  tabletop may fail to move in the horizontal direction when it is commanded to do so during CT scans due to a potential mechanical linkage failure.
Ingenuity CT,  Ingenuity Core, Ingenuity Core 128.
Brilliance iCT SP,  Brilliance iCT,  Brilliance 64,  Brilliance 40, Brilliance 16,  Brilliance 16P, Brilliance 10, Brilliance 6,  Brilliance Big Bore.
Worldwide Distribution - US (Nationwide) and Internationally to Finland and Austria.
SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices.  SURESOUND22 Multipack (OUS Distribution) containing 2 packs of six devices.    For uterine sound
Breach in sterile barrier compromising product sterility
Lot Code US:  16E25RC  16E25RD  16F16R    Lot Code OUS:  16E25RB
Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria,  NDC 0409-7332-01
Sandoz - Lot GJ7151(Pfizer- Lot 670028M); Exp. 07/19
Synthes Flexible Shaft, Orthopedic manual surgical instrument    The Flexible shafts are intended for use as an optional reaming step in intramedullary nailing systems.
Handheld Base Unit for CoaguChek XS Plus and CoaguChek XS Pro Systems
CoaguChek XS Pro and CoaguChek XS Plus Handheld Base Units 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). In case of a patient mismatch, taking into account the difficulty in detecting the issue, the potential for a serious medical adverse event cannot be excluded.  The issue will only occur at sites using POTCT1-A communication via USB.
Handheld Base Unit Product catalog number:  04805658160  All Units in Serial Number Range:  UU00007003 through UU00018502
Amoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan, NDC 0143-9887-01
Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.
Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 60045, NDC 0409-4093-32
Lack of Assurance of Sterility: Complaints of broken tips on the ampules.
Diltiazem HCl Extended-release Capsules, USP 120 mg, 100-count bottle (NDC 0378-5220-01), 500-count bottle (NDC 0378-5220-05), Rx Only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV, 26505 USA
Failed Impurities/Degradation Specifications: OOS results for known compound.
US Distribution to the states of :  CA, FL, GA, MA, MN, NC, NJ, OH, PA and SC.
The Hemotherm 400CE 115v, containing power board p/n 39945
The device may not maintain water flow or temperature control.
Aquilion Prime TSX-303A  Aquilion PRIME is a multislice helical CT system with an 40-row detector. High-speed rotation allows rapid data acquisition and shortens scan times, while the fast reconstruction unit further improves throughput, reducing the time required for diagnosis.
Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system because it  has been reported that the cooling oil in the x-ray tube heat exchanger may leak during system operation.
Nationwide. No Canadian, other foreign, or VA/govt/military consignees.
Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged in 2 Cups. Net weight 1.5 oz (45g) and 1 Cup. Net weight 0.75 oz (21g)
Free2b Foods recalled the Sun Cups Chocolate due to potential contamination with milk ingredients.
LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by:  King Pharmaceuticals, Inc., Bristol, TN 37620, NDC 60793-860-01
BuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 300 mg,  Rx Only, 500-count bottles,  Manufactured by Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA inc. Pennington, NJ 08534, NDC 68382-354-05
Failed Dissolution Specifications: Product did not meet dissolution specification at an intermediate time point.
Lactulose Solution, USP, 10 g/15 mL, 15 mL unit dose cups (NDC 66689-039-01), packaged in 15 mL x 50 unit dose cups per case (NDC 66689-039-50), Rx only, Manufactured by VistaPharm, Inc., Largo, FL 33771.
Microbial Contamination of Non-Sterile Products: bulk solution tested positive for the presence of the bacteria, Burkholderia cepacia.
NJ and further distributed Nationwide in the USA.
KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g), 15 g bottle, Physician Sample: Not For Sale, Rx only, RANBAXY, Jacksonville, FL  32257, UPC 3 10631 09335 8.
Failed Stability Specifications: Low Out of Specification results for alcohol content.
Lot: GHEN, GLGL, GLGL-1, Exp 10/31/2016; HACS, HACS-1, HAFK, HAFK-1, Exp 1/31/2017; HDBB, HDBB-1, HDFS, HDFS-1, Exp 4/30/2017; HFDP, HFDP-1, Exp 6/30/2017