Archive
908 recalls were announced in November 2014.
Of the 908 recalls this month scored against our rubric, 2% are Critical, 20% are Severe.
Which agencies issued them
Daimler Trucks North America is recalling 2013-2015 Thomas Built Buses Minotour school buses because a loose fuel tank strap fastener could cause a fuel leak and fire.
Daimler Trucks North America is recalling 1,580 model year 2015 trucks because an improperly seated brake chamber diaphragm may cause brake drag, increasing the risk of a crash.
Daimler Trucks North America is recalling 2013-2015 Thomas Built Buses Minotour non-school buses because a loose fuel tank strap may allow the tank to contact the ground, increasing the risk of a fuel leak and fire.
Nissan is recalling specific 2012-2015 Nissan Juke and Infiniti models because loose fuel pressure sensors may cause fuel leaks and potential fires.
Abrams Royal Pharmacy is recalling 50 syringes of a compounded lidocaine and bupivacaine mixture due to non-sterility. The products were distributed in Texas.
M & M Farm Inc. is recalling 30,000 lbs of M & M brand Number 2 Florida Avocados because FDA samples tested positive for Salmonella.
Abrams Royal Pharmacy is recalling 1,100 vials of Calcium Chloride Preservative Free Sterile Injection because contract testing found sterility failures.
New Hope Mills is recalling its Gluten Free Chia Pancake and Waffle Mix because it contains undeclared soy.
Abrams Royal Pharmacy is recalling Trace Mineral-5 MDV vials because a contract laboratory identified Staphylococcus warneri in the product, indicating non-sterility.
Unity Groves Corporation is recalling avocados because FDA samples tested positive for Salmonella. The product was distributed in Florida and Texas.
Welcome Market Inc is recalling Coconut Toast products due to missing allergen statements for wheat, soy, and/or milk. The recall affects 3,133 loaves sold in Northern California and Washington.
Karlsburger Foods is recalling InHarvest Garden Vegetable Seasoning due to an undeclared milk allergen. The recall affects 25,651 packets distributed in California.
Allied Recreation Group is recalling 2014-2015 Fleetwood Excursion and 2015 Holiday Rambler Ambassador vehicles because seat mounting brackets may be incorrectly installed, increasing crash injury risk.
Micro Labs USA is recalling 1,440 bottles of Losartan Potassium 25 mg tablets because the dry mix failed blend uniformity specifications.
Biomet Spine is voluntarily recalling 120 Durango Anchored ALIF Plate units because the set screw component may become dislodged from the plate assembly.
Mt. Olive Pickle Company is recalling Kosher Dill Chips in 1-gallon glass jars because they may contain glass fragments. Consumers should check production codes and stop using the product.
Lundberg Sea Salt Rice Chips are being recalled because a customer found a ranch-flavored chip containing dairy in the package.
John Vena, Inc. is recalling raw Serrano peppers packed in white cardboard boxes in Pennsylvania. The peppers were repacked from a product currently being recalled by Bailey Farms.
Nidek Inc is recalling 14 EC-5000 CXIII Excimer Laser Corneal Surgery Systems because a contact failure in fuse holders could cause serious adverse events for patients.
Blooming Import Inc. is recalling Golden Lion brand dried dates due to undeclared sulfites. The product was distributed in ten states.
Accuray is recalling 84 CyberKnife Robotic Radiosurgery Systems to correct a potential safety issue related to upgrading the Treatment Delivery Software for the first generation IRIS Variable Aperture Collimator.
Original Soup Man is recalling Lobster Bisque due to undeclared shrimp, tilapia, and perch. Consumers should check lot numbers and stop consuming the product.
Medtronic Navigation is recalling 26,674 single-use disposable devices because returned items were not adequately inspected for damage that could compromise sterility.
Medtronic Navigation is recalling sterile mouse bags because returned devices may not have been properly examined for damage that could compromise sterility.
Welcome Market Inc is recalling Cheese Toast products sold at 99 Ranch Market in Northern California and Washington due to missing allergen statements for wheat, soy, and milk.
Welcome Market Inc is recalling U-TA-NE Toast products because they lack required allergen statements for wheat, soy, and/or milk.
InHarvest, Inc. is recalling Caviar Medley Garden Vegetable products because the seasoning mix contains undeclared milk.
Medtronic Navigation is recalling 26,674 single-use Ref Frame Driver Kits because returned devices may not have been properly examined for damage to ensure sterility.
Medtronic Navigation is recalling 26,674 disposable sterile devices because returned units may not have been properly examined for damage that could compromise sterility.
Medtronic Navigation is recalling 26,674 biopsy needle kits because returned devices may not have been properly examined for damage to ensure sterility.
InHarvest, Inc. is recalling Rio Medley Garden Vegetable Seasoning because it contains milk, which is not declared on the label.
Owens & Minor is recalling MediChoice Dual-Release Folding Walkers because the wheels may be loose, too tight, or fall off.
Medtronic Navigation is recalling 26,674 sterile percutaneous pins because returned devices may not have been properly examined for damage to ensure sterility.
Taylor Farms is recalling Wawa Garden Rotini and Kale & Quinoa Salads due to potential undeclared fish, wheat, and egg allergens.
Saxon Cheese LLC is recalling one lot of Greenfields Monastery Washed Rind Wisconsin Handcrafted Cheese because the product tested positive for E. coli.
Medtronic Navigation is recalling 26,674 sterile O-Arm drapes because returned devices were not adequately examined for damage to ensure sterility.
Welcome Market Inc is recalling Red Bean Toast products due to missing allergen statements for wheat, soy, and/or milk.
Silver Star Brands is recalling Transport Chair and Rollator units because the wheel assembly may fail, resulting in damaged wheels.
Nidek Inc is recalling 21 MC-500 Multicolor Laser Photocoagulators because the devices may fail to emit laser light or output lower power than programmed during retinal treatment.
Medtronic Navigation is recalling 26,674 Tumor Resection Kits because returned devices may not have been properly examined for damage to ensure sterility.
Medtronic Navigation is recalling 26,674 single-use, disposable navigation devices because returned units were not adequately examined for damage that could compromise sterility.
Welcome Market Inc is recalling various varieties of Pineapple Toast due to missing allergen statements for wheat, soy, and/or milk. The products were sold at 99 Ranch Market in Milpitas, CA.
Welcome Market Inc is recalling Raisin Toast products because they lack required statements for wheat, soy, and/or milk allergens.
Toyota is recalling 25,551 model year 2015 Sienna vehicles because second-row overhead assist grips may detach during curtain airbag deployment, posing an injury risk.
Siemens is recalling six SimView NT simulation systems because a rare defect may prevent components from stopping, risking collision with patients or equipment.
Monteris Medical is recalling 133 FullFire Diffusing Tip Laser Probes because the distal sapphire tip may separate from the probe.
Various toast varieties are recalled because they lack required allergen statements for wheat, soy, and milk. Consumers should discard these products.
Synthes, Inc. is recalling six sterile titanium trochanteric fixation nails due to incorrect assembly that may compromise bone stability.
Elekta, Inc. is recalling 15 units of the MOSAIQ oncology information system because a dose rounding error may cause incorrect numeric data to be displayed on printed reports.
Medtronic Navigation is recalling single-use, disposable devices because returned items were not adequately examined for damage to ensure sterility.
Welcome Market Inc is recalling Taro Toast products because they lack required statements for wheat, soy, and/or milk allergens.
Medtronic Navigation is recalling 26,674 non-invasive shunt kits because returned devices were not adequately inspected for damage that could compromise sterility.
Medtronic Navigation is recalling 26,674 single-use spine pedicle accessory kits because returned devices may not have been properly examined for damage to ensure sterility.
Cycle Gear is recalling specific Street & Steel Brotherhood and Anarchy motorcycle helmets that may not meet federal safety standards for impact protection.
Welcome Market Inc is recalling Wheat Bran Toast products because they lack required statements for wheat, soy, and/or milk allergens.
Monteris Medical is recalling 234 SideFire Directional Laser Probes because the distal sapphire tip may separate from the probe.
Soma Access Systems is recalling 3,530 units of AxoTrack I Sterile Procedure Kits because the sterile packaging may fail before the expiration date.
Medtronic Navigation is recalling single-use instrument trackers because returned devices may not have been properly examined for damage to ensure sterility.
Welcome Market Inc is recalling Green Onion Pork Sung Toast sold at 99 Ranch Market in Northern California and Washington due to missing allergen statements for wheat, soy, and milk.
Medtronic Navigation is recalling single-use Patient Tracker devices because returned units may not have been properly examined for damage to ensure sterility.
InHarvest, Inc. is recalling Garden Vegetable Seasoning Mix because it contains milk, which is not declared on the label.
InHarvest is recalling Garden Vegetable Seasoning because it contains milk, which is not declared on the label.
Welcome Market Inc is recalling various varieties of Family Toast due to missing allergen statements for wheat, soy, and/or milk.
Medacta USA is recalling 32 MectaLIF Oblique Handles because incorrect laser markings could lead to improper device insertion during surgery.
InHarvest, Inc. is recalling Garden Vegetable Seasoning mix because it contains milk, which is not declared on the label.
Medtronic Navigation is recalling 26,674 AxIEM CR tumor resection devices because returned units may not have been properly inspected for damage that could compromise sterility.
Edwards Lifesciences is recalling Vent Catheters because the white plastic coating on the stylet may disrupt. The action covers 157,305 units distributed worldwide.
Medtronic Navigation is recalling 26,674 Tumor Resection Kits because returned devices may not have been properly examined for damage to ensure sterility.
Spectrum Laboratory Products is recalling 16 bottles of Tetrahydrozoline Hydrochloride, USP, 1 KG Bottle, due to storage in a non-GMP compliant warehouse.
Medtronic Navigation is recalling 26,674 Traj Guide Kits because returned devices may not have been properly inspected for damage that could compromise sterility.
Formulations For Life is recalling Resevera Action High Potency Longevity Complex dietary supplements due to lack of Good Manufacturing Practices and misbranding.
Medtronic Navigation is recalling 26,674 sterile drill bits because returned devices may not have been properly examined for damage that could compromise sterility.
Medtronic Navigation is recalling 26,674 thoracic tactile probe kits because returned devices may not have been properly examined for damage to ensure sterility.
Medtronic Navigation is recalling single-use, disposable devices because returned items were not adequately inspected for damage that could compromise sterility.
Medtronic Navigation is recalling 26,674 sterile O-Arm devices because returned units may not have been properly inspected for damage that could compromise sterility.
Nidek Inc is recalling five MC-500 Multicolor Laser Photocoagulators because an engineering change order regarding a memory function problem was not reported as required.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Cleaning Solution because its stability is not assured. The product is used in in vitro diagnostic systems.
Medtronic Navigation is recalling 26,674 ENT PRGM 9734636 ADD FUSION NAV AxiEM devices because returned units may not have been properly examined for damage to ensure sterility.
Prometheus Laboratories is recalling Mercaptopurine Tablets 50mg because the product failed dissolution specifications during stability testing.
Medtronic Navigation is recalling 26,674 sterile percutaneous pins because returned devices may not have been properly examined for damage to ensure sterility.
Medtronic Navigation is recalling 26,674 Traj Guide Kits because returned devices may not have been properly inspected for damage that could compromise sterility.
Formulations For Life is recalling GENE STRENGTH Purple Longevity dietary supplements due to lack of Good Manufacturing Practices and misbranding.
Medtronic Navigation is recalling 26,674 AxiEM Tumor Resonance Packs because returned devices may not have been properly examined for damage to ensure sterility.
Formulations For Life is recalling Vision Assure Extra Strength Vision Formula dietary supplements due to lack of Good Manufacturing Practices and misbranding.
Biomerieux is recalling 652 Etest Ceftaroline devices because the labeling displays a 5-year expiration period instead of the correct 2-year period.
Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration date instead of the correct 2-year date.
Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration instead of 2 years.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur BNP Assay reagents because approximately 2,000 ReadyPacks contain an incorrect human-readable side label.
Biomerieux is recalling 652 Etest Ceftaroline devices because the labeling displays a 5-year expiration instead of the correct 2-year period.
Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration date instead of the correct 2-year date.
Masiero Brothers LLC is voluntarily recalling Oven Fresh Lemon Pound Cake due to misbranding. The product was distributed in New York.
Hospira Inc. is recalling 316,640 vials of Vancomycin Hydrochloride for Injection because product trays were mislabeled to contain a different product.
Goal Zero is recalling Sherpa 50 and 120 rechargeable battery packs because they can overheat and catch fire. Consumers should stop using the units and contact the company for a free replacement.
Yamaha is recalling 2013-2015 XT250 motorcycles because the air induction hose may melt, causing the engine to stall and increasing crash risk.
Aston Martin is recalling 7,256 vehicles because a faulty seat heater module may prevent the heaters from turning off, creating a risk of overheating and injury.
Pro Armor is recalling about 300 utility vehicle doors for Polaris RZR models because the latch pin can disengage, posing impact and laceration hazards.
Spartan is recalling 2013-2015 trucks because damaged air brake valves may reduce braking performance or cause parking brakes to reapply, increasing crash risk.
Capacity is recalling 2014 ISB13 trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.
Harley-Davidson is recalling 1,560 model year 2015 Tri-Glide motorcycles because a defective rear brake master cylinder piston may cause brake failure and increase crash risk.
Champion is recalling 2014-2015 transit buses because defective spring nuts may fail to secure passenger seats, increasing injury risk in a crash.
Looking for a different month? Back to 2014.