Archive
806 recalls were announced in December 2016.
Of the 806 recalls this month scored against our rubric, 13% are Critical, 22% are Severe.
Which agencies issued them
Kuster's Inc. is voluntarily recalling PepperJack cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.
Kuster's Inc. is voluntarily recalling Fata's Best Four Blend Feather Shred Shredded Cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.
Kuster's Inc. is voluntarily recalling shredded, sliced, and cubed cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.
Island Soups Company Inc. is recalling Red Peas Soup due to possible contamination with Clostridium botulinum. Consumers should check their pantry for affected cans.
Heartland is recalling 2016-2017 Landmark 365 fifth wheel trailers because the spare wheel may rub against the brake line, causing wear and potential loss of braking.
Island Soups Company Inc. is recalling Gungo Peas Soup No Meat due to possible contamination with Clostridium botulinum.
Kuster's Inc. is voluntarily recalling 363 lbs of Pepper Jack cut cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.
Autoliv is recalling specific seat belt and air bag initiators that may fail to deploy in a crash due to an improper chemical mix.
Kuster's Inc. is voluntarily recalling Fata's Best Monterey Jack shredded cheese due to potential Listeria contamination or inadequate pasteurization.
Elekta is recalling 671 Monaco RTP Systems because the reset function may calculate an incorrect dose for external beam radiation therapy plans.
Kuster's Inc. is voluntarily recalling sliced Colby Jack cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.
Island Soups Company Inc. is recalling Fish Soup due to possible contamination with Clostridium botulinum. The product was distributed nationwide via internet orders.
Island Soups Company Inc. is recalling Gungo Peas Soup due to possible contamination with Clostridium botulinum. The product was distributed nationwide via internet orders.
Ascend Laboratories LLC is recalling 1,739 bottles of Metformin Hydrochloride 500 mg tablets because Amlodipine tablets were found in the packaging.
Island Soups Company Inc. is recalling Red Peas Soup No Meat due to possible contamination with Clostridium botulinum.
Island Soups Company Inc. is recalling Mannish Water soup due to possible contamination with Clostridium botulinum. Products were sold nationwide via internet orders.
Cadila Pharmaceuticals is recalling bulk Ondansetron HCI API due to microbial contamination. The affected product was distributed to two US consignees.
Daimler Trucks is recalling 2008-2009 Sterling Bullet 4500 and 5500 cab chassis vehicles because a short circuit in the alternator may increase the risk of a fire.
Roche is recalling 97 MSS Cassette units for the OMNI S Analyzer due to a software error that may cause incorrect urea results, potentially delaying diagnosis of inborn disorders in children.
Benson's Old Home Kitchens is recalling Winn Dixie Cream Cheese Creme Cake because it contains undeclared peanut protein, a major allergen.
Teleflex Medical is recalling specific lots of Arrow OnControl Ported Aspiration System Trays because the outer sterile package may have an incomplete seal.
Benson's Old Home Kitchens is recalling specific Lemon Creme Cake products because they contain undeclared peanut protein, a major food allergen.
Hamilton Medical is recalling 44 MR1 ventilators because the oxygen tubing and connector could become loose during preparation, potentially compromising ventilation support.
Teleflex Medical is recalling Arrow OnControl Bone Lesion Biopsy System trays due to a potential incomplete seal on the outer sterile package.
Kuster's Inc. is voluntarily recalling specific lots of shredded cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.
Benson's Old Home Kitchens is recalling 14 oz. Strawberry Swirl Cream Cakes due to undeclared peanut protein. Consumers should not eat the product.
Benson's Old Home Kitchens is recalling Winn Dixie Sock It To Me Creme Cake because it contains undeclared peanut protein.
Kuster's Inc. is voluntarily recalling specific 5 lb. packages of Three Blend Shredded Cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.
Benson's Old Home Kitchens is recalling 28-ounce Dutch Apple Creme Cakes because they contain undeclared peanut protein. The product was distributed in nine states.
Benson's Old Home Kitchens is recalling Winn Dixie 32 oz. Sour Cream Creme Cake because it contains undeclared peanut protein.
MicroPort Orthopedics is recalling 6,250 Dynasty Liners used in hip replacements due to an increasing trend of suspected tissue reactions to metal debris.
Benson's Old Home Kitchens is recalling specific Winn Dixie and Old Home Kitchens vanilla cream cakes because they contain undeclared peanut protein.
Domain Surgical is recalling FMsealer Open Shears (Model FM3001) because fixed jaw fractures were observed during clinical usage.
Mel-O Cream Donuts International, Inc. is recalling specific batches of Star Shaped Shells because a human fingertip was found in the product filling line.
Mel-O Cream Donuts International is recalling Jumbo Apple Fritters because a human fingertip was found in the product filling line.
Rosa Foods is recalling Soylent Food Bars because customers reported gastrointestinal issues after consuming the product.
Purely Elizabeth is recalling Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin, posing a risk to individuals with soy allergies.
Mel-O Cream Donuts International is recalling Jumbo Ring Donuts because a human fingertip was found in the product filling line.
Par Pharmaceutical is recalling specific lots of Travoprost Ophthalmic Solution because the dropper tips may be damaged, compromising sterility.
Greatbatch Medical is recalling Standard Offset Cup Impactors with POM-C handle grips because they failed sterility testing when sterilized according to the Instructions for Use.
B. Braun Medical is recalling 15,950 Sterile IV Start Kits because non-routine sterility testing returned positive results.
Schurman Retail Group is recalling VIVID Red Wine Crush Gift Boxes because mold may be present on the boxes, posing a risk of respiratory irritation.
Teleflex Medical is recalling OnControl Biopsy System Ported Needle Trays due to a potential incomplete seal on the outer sterile package.
MicroPort Orthopedics is recalling Conserve Cups because revision rate trends indicate a specific hazard of tissue reaction to metal debris.
MicroPort Orthopedics is recalling Conserve hip shells because revision rate trends indicate a specific hazard of tissue reaction to metal debris.
Merge Healthcare is recalling Merge Hemo software versions 9.10 through 9.40.2 because the application may crash during cardiac catheterization procedures.
Teleflex Medical is recalling Arrow OnControl Bone Marrow Biopsy Systems due to a potential incomplete seal on the outer sterile package.
MicroPort Orthopedics is recalling 22 Lineage Shell units due to an increasing trend in revision rates and a specific hazard of tissue reaction to metal debris.
Burel Pharmaceuticals is recalling specific lots of Phenazopyridine Hydrochloride Tablets due to manufacturing deviations that may result in assay or content uniformity failures.
MicroPort Orthopedics is recalling 500 units of Procotyl Rim-Lock Liners because revision rate trends indicate a specific hazard of tissue reaction to metal debris.
Burel Pharmaceuticals is recalling AZUPHEN MB Urinary Antiseptic Capsules due to manufacturing deviations that may cause assay or content uniformity failures.
Synthes (USA) Products LLC is recalling 84 units of 0.76 mm Drill Bits that may be incorrectly labeled and actually contain 1.1 mm drill bits.
Spectranetics is voluntarily recalling the Turbo Elite Atherectomy Catheter, ELCA Coronary Atherectomy Catheter, and Bridge Occlusion Balloon because their outer sterile packaging may be compromised.
ConforMIS is recalling two sterile iTotal Knee Replacement Systems distributed to Colorado and Nevada due to incorrect serial numbers on the F4 A/P cut guide iJig.
Terumo Medical Corp is recalling 7,965 MISAGO RX Self Expanding Peripheral Stents nationwide because they do not conform to product specifications regarding diameter and shape.
Baxter Healthcare is recalling 439 V6 Rear Case Assemblies for SIGMA Spectrum Infusion Pumps because the speakers may fail prematurely.
Terumo BCT is voluntarily recalling 660 units of the Adiprep Adipose Transfer System because incorrect labeling could cause operator confusion.
Spectranetics is voluntarily recalling Turbo Elite Atherectomy Catheters and related devices because their outer sterile packaging may be compromised.
Spectranetics is voluntarily recalling ELCA Coronary Atherectomy Catheters and related devices because their outer sterile packaging may be compromised.
Nationwide Laboratories is recalling Phenazopyridine Hydrochloride Tablets due to manufacturing deviations that may result in assay or content uniformity failures.
Mel-O Cream Donuts International is recalling specific batches of Fried Danish because a human fingertip was found in the product filling line.
Teleflex Medical is recalling 113,647 units of Arrow OnControl Bone Marrow Biopsy System Trays due to a potential incomplete seal on the outer sterile package.
Baxter Healthcare is recalling 5,976 Sigma Spectrum Infusion Pumps because some speakers may fail prematurely, potentially affecting audible alarms.
Merge Healthcare is recalling Merge FlexConnect software version 1.0 because communication protocols were not properly handled, preventing data from being processed by the LIS software.
Nationwide Laboratories is recalling Salsalate Tablets, 750 mg, because they were manufactured under practices that may result in assay or content uniformity failures.
Siemens is recalling 33 Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems because the material covering the articulating section has deteriorated, causing acquisition errors.
Sorin Group USA is recalling Stöckert Heater Cooler System 3T units to ensure strict adherence to disinfection and monitoring instructions.
Baxter is recalling SIGMA Spectrum Infusion Pumps to replace speakers that may fail prematurely, potentially affecting audible alarm tones.
Mel-O Cream Donuts International is recalling 20 cases of Arrowhead/Christmas Tree Shells because a human fingertip was found in the product filling line.
MicroPort Orthopedics is recalling 5,009 Lineage Liners used with Conserve metal heads due to a suspected tissue reaction to metal debris.
Burel Pharmaceuticals is recalling Uramit MB Urinary Antiseptic Capsules due to manufacturing deviations that may cause assay or content uniformity failures.
Nationwide Laboratories LLC is recalling Phenazopyridine Hydrochloride Tablets, 200 mg, due to manufacturing deviations that may result in assay or content uniformity failures.
Elekta, Inc. is recalling the Monaco TRP System software because it may incorrectly handle CT datasets with specific DICOM Z coordinates, potentially affecting treatment plan accuracy.
Burel Pharmaceuticals is recalling UROLET MB Urinary Antiseptic tablets because manufacturing deficiencies may cause the product to fail potency or uniformity tests.
Mel-O Cream Donuts International is recalling specific batches of Hy Vee Shells (Bavarian Filled) because a human fingertip was found in the product filling line.
Mel-O Cream Donuts International is recalling specific batches of Hy Vee Long Johns because a human fingertip was found in the product filling line.
Burel Pharmaceuticals is recalling 795 bottles of Indiomin MB capsules due to manufacturing deviations that may cause assay or content uniformity failures.
Mel-O Cream Donuts International is recalling Jumbo Pershing Cinnamon Rolls because a human fingertip was found in the product filling line.
Burel Pharmaceuticals is recalling 17,788 bottles of Phenazopyridine Hydrochloride Tablets due to manufacturing deviations that may cause assay or content uniformity failures.
Burel Pharmaceuticals is recalling 2,861 bottles of Hyolev MB Urinary Antiseptic Tablets due to manufacturing deviations that may cause assay or content uniformity failures.
Nationwide Laboratories is recalling Salsalate Tablets, USP, 500 mg, because they were manufactured under practices that may result in assay or content uniformity failures.
Mel-O Cream Donuts International is recalling Hy Vee Long Shells because a human fingertip was found in the product filling line.
Burel Pharmaceuticals is recalling UROPHEN MB Urinary Antiseptic Tablets due to manufacturing deviations that may cause assay or content uniformity failures.
MicroPort Orthopedics is recalling specific Cobalt Chromium hip replacement heads because internal data showed an increasing trend in revision rates and a specific hazard of tissue reaction to metal debris.
Tesla is recalling specific Universal Mobile Connector Adapters because insufficient welds may cause overheating or arcing, increasing the risk of a fire.
Suzuki is recalling 2012-2016 DL650 motorcycles because a defective stator may cause an engine stall, increasing the risk of a crash.
Indian Motorcycle is recalling 2014-2017 models because the fuel rail may contact other components, causing a fuel leak that increases fire risk.
Target is recalling clear acrylic Hanukkah menorahs that can melt when candles are burning, posing a fire hazard. Consumers should stop using the products and return them for a refund.
Atrium is recalling about 580 SafeHarbor vinyl impact windows because the glass can separate from the frame during hurricanes, posing an impact injury hazard.
Ford is recalling 2017 Fusion vehicles because improperly welded left rear seat back pivot pins may fail in a crash, allowing luggage to move into the passenger compartment.
Hickory Springs is recalling specific Phantomizer 19-inch conversion van seats because the slide tracks may not engage properly, increasing injury risk in a crash.
Entegra is recalling 125 2017 Cornerstone vehicles because the collision mitigation system may be installed upside down, reducing its functionality and increasing crash risk.
Ford is recalling specific 2013-2016 Fusion and 2013-2015 Lincoln MKZ vehicles because heat from seat belt pretensioners may cause anchor cables to fail, increasing injury risk in a crash.
PACCAR is recalling 2017 Peterbilt trucks because brake lights may not illuminate when brakes are applied, increasing crash risk.
National Steak and Poultry is recalling approximately 1.99 million pounds of ready-to-eat chicken products due to possible undercooking, which may allow bacterial pathogens to survive.
General Motors is recalling 2017 Chevrolet Malibus because the right-hand rear side air bag inflator manifold may have insufficient welds, posing a risk of debris or failure during a crash.
General Motors is recalling 2010-2014 Chevrolet Tahoe Police Pursuit vehicles because a cooling fan defect may cause an electrical short and fire.
Thor Motor Coach is recalling 32 model year 2017 Quantum RQ29 motorhomes because they may be missing a required mid-ship marker light, which can increase crash risk.
Forest River is recalling 2017 Puma trailers because incorrect Federal placards list wrong tire and rim information, which could lead to under-inflation and increased crash risk.
Mitsubishi is recalling 2011-2012 and 2016 Outlander Sport vehicles because the lift gate support tube may corrode, causing the gate to fall suddenly and increase injury risk.
Looking for a different month? Back to 2016.