Archive
863 recalls were announced in August 2018.
Of the 863 recalls this month scored against our rubric, 3% are Critical, 25% are Severe.
Which agencies issued them
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
Major Pharmaceuticals is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications.
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling GU Energy Gels because testing confirmed the presence of cyclamates, an ingredient not declared on the label.
Advanced Food Concepts is recalling GU Energy Gels in Caramel Macchiato flavor because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the presence of cyclamates, an unapproved food additive.
Apogee Foods is recalling Thunderbird Apple Pie Kid Bars because the manufacturing process did not reach required temperatures. The product was distributed in Texas.
Advanced Food Concepts is recalling GU Energy Gels in Birthday Cake flavor because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling GU Energy Gels in Toasted Marshmallow flavor because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
West-Ward Columbus Inc is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications.
Hetero Labs is recalling 18,288 bottles of Indomethacin 50 mg capsules due to customer complaints of deformed, clumped, or stuck together capsules.
Envoy Medical is recalling four Esteem II Sound Processors because the sterile wipes inside expired before the date labeled on the final pack.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the presence of cyclamates, an unapproved food additive.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the product may contain cyclamates, an unapproved food additive.
Advanced Food Concepts is recalling GU Energy Gels in Caramel Macchiato flavor because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling GU Energy Gels because testing confirmed the presence of cyclamates, an ingredient not listed on the label.
ELITech Clinical Systems is recalling ENVOY 500 ISE Calibrator Kits because some vials cause calibration errors, delaying patient results.
Frito-Lay is recalling specific 8.5 oz bags of Ruffles Cheddar and Sour Cream potato chips due to a potential for cleaning solution to come into contact with the product.
Frito-Lay is recalling approximately 129 bags of Ruffles Original potato chips sold in Northeastern Ohio and Altoona, PA, due to a potential for cleaning solution contact.
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling Roctane Ultra Endurance BCAA Capsules because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
Apogee Foods is recalling Thunderbird Bars because the manufacturing process did not reach required temperatures. The recall affects 63 cases distributed in Texas.
Holmquist Hazelnut Orchards is recalling Ranch Flavored Hazelnuts in 4 oz, 6 oz, and 1 lb sizes due to an undeclared hazelnut allergen in the product's 'Contains' statement.
Advanced Food Concepts is recalling GU Energy Gels because testing confirmed the presence of cyclamates, an ingredient not declared on the label.
Advanced Food Concepts is recalling GU Energy Gels because testing confirmed the presence of cyclamates, a substance not permitted in the product.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the presence of cyclamates, an ingredient not declared on the label.
PepsiCo is recalling Diet Pepsi 7.5 oz 6-packs in five western states because the product contains undeclared aspartame.
Sugar Foods Corporation is recalling Old Chicago Basil Pesto Croutons because the whey powder used in their production was subject to a recall.
Advanced Food Concepts is recalling Roctane Ultra Endurance Energy Gels because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling GU Energy Chews because testing confirmed the presence of cyclamates, an ingredient not declared on the label.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the product may contain cyclamates, an ingredient not permitted in food.
Advanced Food Concepts is recalling GU Energy Gels (Campfire Smores) because testing confirmed the presence of cyclamates.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the presence of cyclamates, an unapproved food additive.
Vensun Pharmaceuticals is recalling 11,652 bottles of Potassium Citrate Extended-Release Tablets because they failed specifications due to tablet breakage.
West-Ward Columbus Inc. is recalling Doxycycline Hyclate 100 mg tablets because they failed dissolution specifications.
Howmedica is recalling five custom implant systems because they lacked updated instructions clarifying the locking mechanism and screw warnings.
Encore Medical is recalling 30 instrument trays used for AltiVate Small Shell Trials because a black coating may appear after cleaning that is not biocompatible.
Diamedix Corporation is recalling 147 units of the Is-EBV-EA-D IgG Enzyme Immunoassay Test Kit due to a gel-like contaminant that may affect product performance.
Diamedix Corporation is recalling 505 units of the Is-Mumps IgG Enzyme Immunoassay Test Kit because a gel-like contaminant may affect product performance.
Lupin Pharmaceuticals is recalling Moxifloxacin Ophthalmic Solution because an out-of-specification result was found in a stability study. The product was distributed throughout the United States.
Renaissance Lakewood, LLC is recalling 3,000 bags of Fluconazole Injection due to elevated sodium chloride and water vapor levels.
Renaissance Lakewood, LLC is recalling Fluconazole Injection bags due to elevated water vapor levels. The recall covers 3,664 bags distributed nationwide and in Puerto Rico.
Becton, Dickinson and Company is recalling 8 BD FACS Universal Loader devices because the solenoid plunger tip is too short to lock securely during use.
Terex is recalling 2015-2018 C4000, C5000, C6000, and General 80 digger derricks because undersized welds may cause the auger to fall unexpectedly, posing an injury risk.
BYD is recalling 2016-2017 K11 M hybrid buses because a brake caliper guide pin may break, potentially causing loss of braking ability or tire pressure.
NEMO Equipment is recalling about 7,500 Stargaze recliner chairs because plastic joint supports can break, posing a fall hazard.
Micro Bird is recalling 2015-2018 G5, MB II, and T-Series transit buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in crashes.
Hale Products Inc is recalling Kubota Diesel Powered Portable Pumps because improper wiring may prevent warning lamps from illuminating, increasing the risk of injury if the engine fails.
Micro Bird is recalling 2015-2018 G5, MB II, and T-Series school buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in a crash.
Newmar is recalling 2018-2019 motorhomes because improperly adjusted door latch rods may allow the entry door to open during transit.
Garden State Bus Group is recalling 2015 Double Deck Buses because the roof emergency exit is incorrectly located, potentially delaying evacuation during an emergency.
StoneRidge Wholesale Division LLC is recalling approximately 656 pounds of pork and beef bologna products because they contain undeclared sodium nitrite and sodium erythorbate.
Mercedes-Benz is recalling 2018 E 400 Cabrio vehicles because the child seat anchoring system may not be properly installed, increasing injury risk in a crash.
Freedman Seating Company is recalling GO-ES Foldaway Seats because the cushion may not stay locked during a crash, increasing injury risk.
Star Natural Meats is recalling raw pork sausage products because they contain undeclared milk, soy, and restricted ingredients.
Mercedes-Benz is recalling 2018 GLE 350 and AMG GLE43 vehicles because the panoramic sunroof may not be properly adhered, creating a road hazard.
Mercedes-Benz is recalling 2018 E-Class and 2019 CLS vehicles because the front passenger air bag may not deactivate if a child seat is installed, increasing injury risk.
Mercedes-Benz is recalling 2018 CLA250 and CLA45 AMG vehicles because the front passenger air bag may fail to deactivate if a child seat is installed.
Honda is recalling Genuine Accessory Centerstand Kits for 2016-2018 Africa Twin motorcycles because a broken circlip can cause the stand to detach, creating a road hazard or causing the bike to fall.
Van Oriental Foods Inc. is recalling pork egg rolls that may contain soft plastic. No illnesses have been reported.
Newmar is recalling 119 motorhomes because brake caliper mounting bolts may be insufficiently tightened, potentially reducing braking performance and increasing crash risk.
Dexter Axle Company is recalling certain trailer axles because incorrect tapered roller bearings may have been installed, increasing the risk of a crash.
Zebra Technologies is expanding a recall of power supply units for thermal printers due to a fire hazard. The units can overheat and catch fire when exposed to moisture.
Subaru is recalling 2019 Ascent vehicles because missing spot welds on the B-Pillar may compromise vehicle strength, increasing the risk of injury in a crash.
Rena Ware is recalling about 700 Nutrex pressure cookers because they can discharge steam at lower pressures than intended, posing a burn hazard.
Textron Specialized Vehicles is recalling about 255 Arctic Cat snowmobiles because the handgrip can break, posing an injury hazard to the rider.
CPSC recalls Hill Topper electric bike motor controllers that may accelerate on their own, posing crash and injury risks to riders.
Miller Fireworks is recalling specific rocket and cracker fireworks that violate federal standards due to explosion and burn hazards.
General Motors is recalling 2018 Chevrolet Express and GMC Savana vans because the tire pressure monitoring system may be incorrectly calibrated, potentially delaying low-pressure warnings.
Thor Motor Coach is recalling 2017-2019 Aria and Venetian motorhomes because brake caliper mounting bolts may loosen, potentially reducing braking performance.
Holley Cold Storage Fruit & Produce Co., Inc. is recalling Europe's Best Field Berry Mix because it may be contaminated with Salmonella.
Tilgner's Alaskan Salmon is recalling Ruby Red Sockeye Candy cold smoked salmon in 4 oz packages due to Listeria monocytogenes contamination.
Holley Cold Storage Fruit & Produce Co., Inc. is recalling Europe's Best 4-Field Berry Mix due to potential Salmonella contamination.
Holley Cold Storage Fruit & Produce Co., Inc. is recalling Europe's Best Bananas & Berries 12/600g in Canada due to potential Salmonella contamination.
Major Pharmaceuticals is recalling specific lots of 160 mg Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Major Pharmaceuticals is recalling specific lots of 80 mg Valsartan tablets because a carcinogen impurity was detected in the active ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan Tablets 40 mg because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc. is recalling Valsartan 40 mg tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc. is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan Tablets 320 mg because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc. is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Tilgner's Alaskan Salmon is recalling Canoodles coarse ground cold smoked dehydrated shelf stable sockeye salmon pieces due to potential Listeria monocytogenes contamination.
Teva Pharmaceuticals is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan Tablets 80 mg because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc. is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Prinston Pharmaceutical Inc is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Cayenne Medical Inc. is recalling specific models of the AperFix Femoral Implant Coring Removal Drill due to a trend of premature wear and breakage identified in 2010.
Prinston Pharmaceutical Inc is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan Tablets 160 mg because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
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