Archive
511 recalls were announced in February 2016.
Of the 511 recalls this month scored against our rubric, 5% are Critical, 31% are Severe.
Which agencies issued them
England's Stove Works is recalling about 2,300 Smartstove freestanding pellet stoves because ash accumulation can cause the door glass to break, posing a laceration hazard.
Crossroads is recalling 2016-2017 Z1 Lite travel trailers because a furnace exhaust cover may mislabel the hot tube location, posing burn and fire risks.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile methylcobalamine injections because an FDA inspection found concerns regarding the assurance of sterility.
Philips is recalling actuator assemblies for angiographic x-ray monitor ceiling suspension systems because the actuator can detach, causing the monitor carriage to drop.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine prostaglandin, after FDA inspection found concerns regarding lack of sterility assurance.
ViewRay is recalling five MRIdian Radiation Therapy Systems because they loaded a completion fraction in the incorrect order after a treatment interruption.
Umpqua Dairy Products Co is recalling Umpqua Mountain Blackberry Revel Ice Cream because the milk used was presumptive positive for beta lactam antibiotics.
Sunset Natural Products Inc. is recalling Prostax Forte dietary supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Red Diamond, Inc. is recalling 22 units of European Roast Coffee Concentrate due to elevated pH levels in an acidified product.
Kwik Trip Bakery is recalling Jelly Bismark products that may contain plastic pieces from contaminated ice nuggets.
Umpqua Dairy Products Co is recalling Peppermint Candy Ice Cream because the milk used was presumptive positive for beta lactam antibiotics.
JNC International Inc. is recalling Little Temptations Sour Strawberries because they contain undeclared FD&C Blue #1 and Yellow #5.
Sunset Natural Products is recalling Prostaliv dietary supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Umpqua Dairy Products is recalling Dairy Queen Chocolate Soft Serve Mix because the milk used was presumptively positive for beta-lactam antibiotics.
Verathon is recalling GlideScope and AVL video laryngoscope reusable blades to update the Operations and Maintenance Manual regarding chemical cleaning cycle limits.
Leica Microsystems is recalling Bond Polymer Refine Red Detection kits due to a manufacturing error that may cause inadequate staining.
Umpqua Dairy Products Co is recalling 160 three-gallon containers of Sunshine Empress Vanilla Ice Cream because the milk used was presumptive positive for beta lactam antibiotics.
Sunset Natural Products Inc. is recalling Argindione capsules pursuant to a consent decree requiring the destruction of supplements manufactured or distributed since April 2, 2014.
Sunset Natural Products Inc. is recalling Moinsage dietary supplement capsules pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
B&D Seafoods is recalling specific lots of frozen swai fillets because they contain nitrofurans, a prohibited veterinary drug.
Lee Food Corporation is recalling Marky's Puto Seko Special because it contains undeclared colors and an unallowable dye.
Umpqua Dairy Products Co is recalling Peppermint Candy Ice Cream because the milk used was presumptive positive for beta lactam antibiotics.
Kwik Trip Bakery is recalling Custard Bismarks that may contain plastic pieces from contaminated ice nuggets used as an ingredient.
Umpqua Dairy is recalling 4% Cottage Cheese because the milk used was presumptively positive for beta-lactam antibiotics without confirmation testing.
Red Diamond, Inc. is recalling 136 units of Colombian Coffee Concentrate due to elevated pH levels in an acidified product.
Kwik Trip Bakery is recalling Triple Choc Bismark products that may contain plastic pieces from contaminated ice nuggets. The recall affects products distributed in Wisconsin, Minnesota, and Iowa.
Kwik Trip Bakery is recalling plain bagels that may contain plastic pieces from contaminated ice nuggets. The products were distributed in Wisconsin, Minnesota, and Iowa.
Umpqua Dairy is recalling nonfat cottage cheese because the milk used was presumptive positive for beta lactam antibiotics.
Bake Rite Rolls Division of Northeast Foods is recalling 100% Whole Grain Hot Dog Rolls due to the possible presence of plastic.
Umpqua Dairy Products Co is recalling Birthday Cake Ice Cream because the milk used was presumptive positive for beta lactam antibiotics.
Kwik Trip Bakery is recalling Cinnamon Cinnsations because they may contain pieces of plastic from contaminated ice nuggets.
Bonita Pharmaceuticals is recalling Menthocin Patch with Lidocaine-Strong because it was marketed without an approved NDA or ANDA.
Sunset Natural Products Inc. is recalling Hepasil dietary supplements under a consent decree requiring the destruction of products distributed since April 2, 2014.
Exactech is recalling 19 Acapella One Interbody Fusion Devices due to incorrect external and internal packaging labels.
Umpqua Dairy Products Co is recalling Lowfat Vanilla Soft Serve Ice Cream Mix because the milk used was presumptively positive for beta-lactam antibiotics.
Kwik Trip Bakery is recalling Filled Long Johns that may contain plastic pieces from contaminated ice nuggets used as an ingredient.
Umpqua Dairy is recalling 1.5% lowfat cottage cheese because the milk used was presumptively positive for beta-lactam antibiotics.
Sorin Group USA is recalling 60 units of Dual Stage Venous Return Catheters because the cases contained incorrect Instructions For Use (IFU).
Kwik Trip Bakery is recalling Cinnamon Raisin Bagels because they may contain pieces of plastic from contaminated ice nuggets.
Umpqua Dairy Products Co is recalling French Vanilla Ice Cream because the milk used was tested presumptive positive for beta lactam antibiotics.
Umpqua Dairy Products Co is recalling cultured sour cream because the milk used was presumptive positive for beta lactam antibiotics.
Sunset Natural Products Inc. is recalling 4,000 bottles of Prostamax DUO dietary supplements in Florida and Nevada pursuant to a consent decree.
Umpqua Dairy Products Co is recalling 400 three-gallon containers of Umpqua Vanilla Ice Cream because the milk used was presumptive positive for beta-lactam antibiotics.
Sunset Natural Products is recalling Abee Med dietary supplements under a consent decree requiring the destruction of products manufactured since April 2014.
B&D Seafoods is recalling frozen swai fillets because they contain nitrofurans, a prohibited veterinary drug.
Sunset Natural Products Inc. is recalling Neuro-Cetin dietary supplements under a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products is recalling Chardon de Marie dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
B&D Seafoods Inc. is recalling frozen swai fillets because they contain nitrofurans. The product was distributed in California and Florida.
Smith & Nephew is recalling 8 units of Legion Hemi Stepped Tibial Wedges because the included screws were too long to properly affix the device.
Dr. Reddy's Laboratories is recalling 9,155 bottles of Paricalcitol capsules nationwide due to reports of breakage and leakage.
Dr. Reddy's Laboratories is recalling Paricalcitol capsules due to reports of breakage and leakage. The recall covers 4,383 bottles distributed nationwide.
C.R. Bard is recalling 15,400 units of 70cc Toomey Syringes because a customer reported an open package seal.
Dr. Reddy's Laboratories is recalling 11,123 bottles of Paricalcitol capsules nationwide because the capsules have broken and leaked.
Lab Vision Corporation is recalling specific lots of CEA/CD66e Ab-2 antibody because they were produced with an incorrect dilution factor.
Kawasaki is recalling 544 model year 2016 Ninja ZX-10R motorcycles because steering damper bracket mounting bolts may break, potentially interfering with steering and increasing crash risk.
Blue Bird is recalling 733 model year 2008-2009 Vision school buses because a wiring defect may cause the battery cable to overheat, melt, and create a fire risk.
Blue Bird is recalling 2009 Vision transit buses with Caterpillar C707 engines because a wiring defect may cause the battery cable to overheat, melt, and create a fire hazard.
Daimler Trucks North America is recalling 2012-2017 Thomas Built Buses Minotour school buses because a body control module failure may cause loss of exterior lighting or windshield wipers.
Ajinomoto Windsor Inc. is recalling approximately 6,000 pounds of Shirakiku Gyoza Dumplings labeled as beef but containing undeclared pork.
Flying Food Group is recalling Starbucks Edamame Hummus Wraps because they may contain undeclared peanuts and tree nuts.
Toyota is recalling 2006-2012 RAV4 and 2012-2014 RAV4 EV vehicles because rear seat belts may be cut by the seat cushion frame in a frontal collision, increasing injury risk.
Mack Trucks is recalling 1,187 model year 2016-2017 Granite and TerraPro trucks because a missing roll pin may cause the steering shaft to disconnect, resulting in a complete loss of steering.
Mack Trucks is recalling 33,981 model year 2012-2016 trucks because a cap nut may loosen, causing the driveshaft to disconnect and increasing crash risk.
Volvo Trucks North America is recalling certain 2009-2010 VT and 2016 VNL/VNM trucks because front suspension drag links may corrode, potentially causing loss of steering.
Daystar is recalling aftermarket rear control arm brackets for 2015-2016 Jeep Renegades due to improper welds that may allow the rear axle to shift, increasing crash risk.
Highland Ridge RV is recalling 2015-2016 travel and fifth wheel trailers because incorrect Gross Vehicle Weight Rating labels may allow overloading, increasing the risk of tire failure and crashes.
Apple is recalling approximately 814,000 travel adapter kits and plug adapters because the two-prong adapters can break and expose metal, posing an electric shock risk.
Daimler Vans USA is recalling 2015-2016 Sprinter vans because tire pressure labels list incorrect maximum load capacities, which could lead to axle or tire failure.
Boa is recalling snowboard boots with M3v2 secondary reels because the mechanism can get stuck, loosening the fit and posing a fall hazard. No injuries have been reported.
Evenflo is recalling specific Transitions 3-in-1 Combination Booster Seats because the harness adjuster button may be within a child's reach, allowing them to loosen the harness and increasing injury risk in a crash.
J. Crew is recalling specific girls' puffer coats because front buttons can detach, posing a choking hazard to young children. No injuries have been reported.
ENVE is recalling about 600 carbon fiber bicycle forks because the left leg can crack, posing a fall hazard. No injuries have been reported.
Navistar is recalling 2016-2017 IC CE school buses because hood straps may elongate, allowing the hood to open unexpectedly during braking and obstructing the driver's vision.
Forest River is recalling 2016 Coachmen Galleria motorhomes because the Federal Placards incorrectly list seatbelts and omit the Gross Vehicle Weight Rating, increasing crash risk.
Raynor Marketing is recalling about 1,200 Eurotech Lume office chairs because the seat can detach, posing a fall hazard. No injuries have been reported.
BYA Sports is recalling Skyline backyard zipline kits because a cable crimp can fail, posing a fall hazard. Consumers should stop using the kits and contact the company for a free replacement.
FreshPoint Corporate is recalling 1,507 cases of whole cucumbers distributed in Florida and Georgia due to possible Salmonella contamination.
E3 Artisan is recalling dark chocolate bars with strawberries, rose petals, and pink peppercorns because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling dark chocolate bars containing cherries, cocoa nibs, and cayenne because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Meltaway bars because FDA samples tested positive for undeclared milk, posing a risk to consumers with milk allergies.
E3 Artisan is recalling Meltaway bar-black cherry lemonade dark chocolate bars because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Meltaways dark chocolate bars because FDA testing found undeclared milk. Consumers with allergies should not consume the product.
E3 Artisan is recalling dark chocolate bars containing strawberries, mangoes, and chiles because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling 30-bar packages of Tahitian Vanilla Lemon Meltaways because FDA testing found undeclared milk on the labels.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, a major food allergen.
Volvo is recalling 2016-2017 VNL, VNX, and VNM trucks because a missing roll pin or loose bolt may cause the steering shaft to separate, resulting in a loss of steering.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk on the labels.
E3 Artisan is recalling 40 bars of 3-piece Blood Orange Meltaways because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, a major food allergen.
E3 Artisan is recalling dark chocolate bars because FDA testing found undeclared milk, a major allergen, in the product.
Pharmedium Services, LLC is recalling 19 syringes of Morphine Sulfate in Wisconsin because the drug was found to be subpotent.
Smith & Nephew is recalling BEAVER Blade 4.0mm orthopedic instruments because they may fracture during hip arthroscopy procedures.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, posing a risk to consumers with milk allergies.
C.R. Bard is recalling Arctic Sun 5000 and 2000 devices because a simulator key could be connected to the patient cable, resulting in improper temperature therapy.
E3 Artisan is recalling specific dark chocolate bars because FDA samples tested positive for undeclared milk, a major allergen.
E3 Artisan is recalling 3-piece peppermint meltaways because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Mendiant Orange apricot and caramelized hazelnut chocolate bars because FDA samples tested positive for undeclared milk.
Philips is recalling two Allura Xper FD OR Tables because the C-arc may continue moving after stopping due to improper adjustment.
FreshPoint Corporate is recalling sliced cucumbers in Florida and Georgia due to possible Salmonella contamination.
E3 Artisan is recalling Mendiant dark chocolate bars because FDA testing found undeclared milk, a major allergen, in the product.
Looking for a different month? Back to 2016.