Archive
622 recalls were announced in April 2018.
Of the 622 recalls this month scored against our rubric, 3% are Critical, 22% are Severe.
Which agencies issued them
Ford is recalling 25,658 2015-2017 Transit vehicles with trailer tow modules because water intrusion can corrode wiring, potentially causing electrical shorts, fires, or crashes.
Altec is recalling 2017-2018 EC175, EC225, and EC655 Boom-Mounted Saw vehicles because a valve may allow tree trunks to slip or fall, increasing injury risk.
Pinnacle Foods Inc. is recalling approximately 32,479 pounds of heat-treated, shelf-stable beef products due to a possible processing deviation that may have led to toxin contamination.
Advance Stores is recalling ToolWorks TW1489 Fuse Kits sold at Advance Auto Parts and Carquest because the fuses may fail to protect circuits, increasing fire risk.
Mercedes-Benz is recalling 2008-2009 Smart Fortwo vehicles because a rear insulation mat may contact hot exhaust components, increasing fire risk.
Forest River is recalling 2018 Starcraft Bus XLT and Glaval Bus Concorde II models because a gear shift cable clip may not be properly seated, potentially causing the vehicle to roll or shift unexpectedly.
Mercedes-Benz is recalling specific 2012-2017 SUVs because oil in the Active Curve System may leak and cause a fire if the level is low.
Mercedes-Benz is recalling 2017 E300, E400, and AMG E43 vehicles because headlight adjustment screws may not be properly sealed, potentially allowing misalignment.
MORryde is recalling 822 Rotational Rubber Pin Boxes because incorrect spindle placement may cause loose bearings, increasing the risk of a crash.
Forest River is recalling 2018 Prime Time WCF35MB trailers because the Federal Placard lists an incorrect Gross Vehicle Weight Rating, which could lead to overloading and increased crash risk.
ZF North America is recalling certain axles with radial air disk brakes because a broken guide pin support bolt may cause loss of braking ability or tire pressure.
Honda is recalling 2017 Civic Hatchback and Type R vehicles because replacement seatback pads may block side air bags, increasing injury risk in a crash.
Honda is recalling various 2001-2012 models because the front passenger air bag may have been installed incorrectly during replacement, increasing injury risk in a crash.
General Motors is recalling certain 2009-2018 Chevrolet, GMC, and Isuzu vehicles because the installed fire extinguishers may clog or detach, potentially failing to function during a fire.
Seacrest Foods International is recalling L'Explorateur soft ripened cheese due to potential Listeria monocytogenes contamination. The product was distributed in Massachusetts, New Hampshire, Maine, and Connecticut.
Club 13 Enterprises Warehouse is recalling specific lots of Kratom Maeng Da Red XS capsules because samples tested positive for Salmonella.
Club 13 Enterprises Warehouse is recalling specific lots of Maeng Da Red powder after testing confirmed the presence of Salmonella.
River Valley Sprouts is recalling garlic and alfalfa sprouts due to the potential for Salmonella contamination. The product was distributed in Minnesota and Wisconsin.
Club 13 Enterprises Warehouse is recalling specific lots of Kratom Maeng Da Red capsules because samples tested positive for Salmonella.
Aspire Food Group is recalling EXO Cricket Protein Bars in Blueberry Vanilla flavor because they contain undeclared sulfites. The recall affects 40,512 units distributed in the United States and Germany.
Global Commodities Corp. is recalling one lot of frozen grated coconut after the California Department of Public Health detected Salmonella.
Nutrizone LLC is recalling all packages of Nirvanio Green Malay Kratom because dietary supplements have the potential to be contaminated with Salmonella.
Aspire Food Group USA Inc. is recalling EXO Cricket Protein Bars in Apple Cinnamon flavor because they contain undeclared sulfites.
Davis Chocolate is voluntarily recalling peanut morsels and organic peanut chips due to Listeria monocytogenes detected by a customer's laboratory analysis.
Nutrizone LLC is recalling all packages of Nirvanio Bali Kratom because dietary supplements may be contaminated with Salmonella.
Philips is recalling 119 Brilliance Big Bore CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.
Partell Specialty Pharmacy is recalling Testosterone 50 mg pellets because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling specific testosterone and hormone pellet vials because they were sterilized using a non-approved method.
River Valley Sprouts is recalling 1,867 lbs of alfalfa sprouts in Minnesota and Wisconsin due to potential Salmonella contamination.
Partell Specialty Pharmacy is recalling Biotin Suspension 10mg/mL vials because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Naltrexone 200 mg pellets because a non-approved sterilization method was used, creating a lack of assurance of sterility.
Autochair is recalling Milford Smartbase units because a weak spring and misaligned locking pin caused legs to fold, dropping a person.
Partell Specialty Pharmacy is recalling Testosterone 100 mg pellets in Nevada because they were sterilized using a non-approved method.
Blue Bird is recalling 2018-2019 All American and Vision transit buses because air brake gauges may incorrectly display 0 PSI, increasing crash risk.
Partell Specialty Pharmacy is recalling specific lots of Testosterone/Anastrozole pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling MVI-7 injectable vials because a non-approved sterilization method was used, raising concerns about product sterility.
Cook Inc. is recalling 132 Cook Vacuum Pumps (K-MAR-5200-US) worldwide due to defective crimp connectors that may cause device failure, electric shock, or burns.
Partell Specialty Pharmacy is recalling Estradiol 50 mg pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling Testosterone 80 mg pellets in Nevada because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Pregnenolone 100 mg pellets because they were sterilized using a non-approved method.
Aspire Food Group is recalling EXO Cricket Protein Bars in Peanut Butter and Jelly flavor because they contain undeclared sulfites. The affected units were distributed in the United States and Germany.
Partell Specialty Pharmacy is recalling specific lots of B-complex injectable vials because a non-approved sterilization method was used.
Lupin Pharmaceuticals is voluntarily recalling 40,824 bottles of Cefdinir powder for oral suspension because the drug was found to be superpotent.
Partell Specialty Pharmacy is recalling Methylcobalamin 12.5 mg/mL Injectable Liquid in Nevada due to a non-approved method of sterilization.
Partell Specialty Pharmacy is recalling Estradiol 35 mg pellets in Nevada due to the use of a non-approved sterilization method.
Partell Specialty Pharmacy is recalling four vials of Glutathione 200mg/mL in Nevada because the products were sterilized using a non-approved method.
Divinity Product Distribution LLC is recalling kratom powder products because the ingredient lacks sufficient safety data to ensure it does not pose a risk of illness or injury.
Partell Specialty Pharmacy is recalling CoEnzymeQ10 25mg/mL vials because they were sterilized using a non-approved method.
Nutrizone LLC is recalling all packages of Pain Out Maeng Da Kratom dietary supplements nationwide due to the potential for Salmonella contamination.
Partell Specialty Pharmacy is recalling Testosterone 37.5 mg pellets because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Nandrolone decanoate 200mg/mL vials because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Testosterone 55 mg pellets in Nevada because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling specific vials of a methionine, inositol, choline, and B12 combination drug due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling Estradiol 25 mg pellets in Nevada because they were sterilized using a non-approved method.
Blue Bird is recalling 2018-2019 Vision and All American school buses because air brake gauges may incorrectly display 0 PSI, increasing crash risk.
Partell Specialty Pharmacy is recalling Testosterone Propionate 100mg/mL vials because a non-approved method of sterilization was used.
Partell Specialty Pharmacy is recalling Testosterone 40 mg pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling specific lots of TM drug vials because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Ascorbic Acid (Tapioca) 500 mg/mL vials because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Vitamin D 50,000 unit/ml injectable liquid because it was sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling TM #1 Injectable solution because a non-approved sterilization method was used. The product was distributed only in Nevada.
Partell Specialty Pharmacy is recalling 7 vials of Testosterone Cypionate 200mg/mL in Nevada because the firm used a non-approved method of sterilization.
Partell Specialty Pharmacy is recalling Testosterone/Anastrozole pellets because they were sterilized using a non-approved method.
Cook Inc. is recalling 2,267 Cook Vacuum Pumps (K-MAR-5200-US) worldwide due to defective crimp connectors that may cause device failure, electric shock, or burns.
Partell Specialty Pharmacy is recalling Testosterone/Finasteride pellets because they were sterilized using a non-approved method.
Divinity Product Distribution LLC is recalling kratom capsules because the ingredient lacks adequate safety information to ensure it does not present a significant risk of illness or injury.
Partell Specialty Pharmacy is recalling Estradiol 20 mg pellets in Nevada because a non-approved sterilization method was used.
Partell Specialty Pharmacy is recalling Testosterone/Finasteride/Anastrozole pellets because they were sterilized using a non-approved method.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because missing hardware may allow the rear ramp to detach while moving, increasing crash risk.
Partell Specialty Pharmacy is recalling TM #4 drug products because a non-approved method of sterilization was used.
Volkswagen is recalling 2018 Tiguan long wheelbase vehicles because a rear shock absorber loop may separate, potentially causing loss of vehicle control.
Nutrizone LLC is recalling all packages of Pain Out Thai Kratom because dietary supplements may be contaminated with Salmonella.
Partell Specialty Pharmacy is recalling Testosterone 200 mg pellets in Nevada because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Testosterone/Anastrozole pellets because a non-approved sterilization method was used, raising concerns about sterility assurance.
Partell Specialty Pharmacy is recalling specific lots of Progesterone 50 mg pellets in Nevada because the products were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Estradiol 12.5 mg pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling Testosterone/Finasteride 80 mg/8 mg pellets because a non-approved method of sterilization was used.
Marcas Usa Llc is recalling specific lots of PASTA DE LASSAR ANDROMACO Skin Protection cream due to microbial contamination.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because ramp-securing bolts may loosen or break, increasing the risk of injury or a crash.
Partell Specialty Pharmacy is recalling Methionine 25mg/Inositol 50mg/Choline 50mg/B12 1mg injections because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Estradiol 55 mg pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling Estradiol 15 mg pellets in Nevada due to a non-approved sterilization method.
Nutrizone LLC is recalling all packages of Nirvanio Special Reserve Kratom because dietary supplements can be contaminated with Salmonella.
Kwik Trip is recalling Kitchen's Cravings Egg Salad Sandwiches because they may contain undeclared fish and shellfish allergens.
Philips is recalling 19 Brilliance iCT SP CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.
Partell Specialty Pharmacy is recalling Lipoic Acid 25mg/mL vials in Nevada because the firm used a non-approved method of sterilization.
Partell Specialty Pharmacy is recalling TM #6 drug products in Nevada due to a non-approved method of sterilization.
Partell Specialty Pharmacy is recalling TM #3 drug vials because they were sterilized using a non-approved method, raising concerns about sterility assurance.
Partell Specialty Pharmacy is recalling Testosterone/Anastrozole pellets in Nevada because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling HCG 1000 units/mL vials in Nevada because a non-approved sterilization method was used.
Nutrizone LLC is recalling all packages of Cali Thai Kratom because dietary supplements may be contaminated with Salmonella.
Halyard Health is recalling certain Closed Suction Systems because Flex Connectors may become loose or disconnect before or during use.
Mrs. Gerry's is recalling various egg and potato salads because they may contain undeclared traces of imitation crab meat.
Midwest Northern Inc. is recalling 35,056 lbs. of Nut Pure Nut Topping due to potential allergen cross-contact in the oil used to roast the nuts and seeds.
Midwest Northern Inc. is recalling Asian Snack Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.
Mrs Gerry's Kitchen is recalling Festival Foods Potato Salad because it may contain undeclared traces of imitation crab meat.
Midwest Northern Inc. is recalling its Nut BBQ Blues Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.
Midwest Northern Inc. is recalling Chopped Mix, Roasted & Salted due to potential allergen cross-contact in the roasting oil.
Midwest Northern Inc. is recalling Redskin Peanuts due to potential allergen cross-contact in the roasting oil. Consumers should stop using the product.
Midwest Northern Inc. is recalling roasted salted almonds due to potential allergen cross-contact in the roasting oil.
Looking for a different month? Back to 2018.