Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Yamaha is recalling 320 model year 2011 Vino Classic motorcycles because brake shoe linings may separate, reducing brake performance and increasing crash risk.
Teva Pharmaceuticals is recalling CARBOplatin Injection because the required reduction of endotoxin was not met during annual revalidation of the vial washer.
The Warrell Corporation is recalling chocolate covered peanuts mislabeled as raisins because the peanut allergen is not identified on the packaging.
Sure Power is recalling battery equalizers and DC-DC converters because a potting compound can conduct electricity and cause fires.
Micro Bird is recalling 2013 G5 school buses because improperly glued ceiling panels may separate in a crash, increasing injury risk.
Goshen Coach is recalling 709 model year 2009 and 2010 buses because voltage spikes may damage door header circuit boards, increasing the risk of fire.
Eldorado is recalling 2010 Aerotech, Aero Elite, and Aerolite buses because voltage spikes in door headers may cause overheating and fire.
Daimler Trucks North America is recalling 2014 Freightliner Cascadia trucks because brake caliper mounting bolts may be incorrectly torqued, potentially leading to reduced brake effectiveness.
Heeren Brothers Produce is recalling Athena cantaloupes sold in Michigan after FDA testing found Listeria monocytogenes contamination.
Hospira is recalling 264,432 bags of 0.9% Sodium Chloride Injection because the product may contain fibrous material.
Advance Pharmaceutical Inc. is recalling 16,440 bottles of Enteric Coated Aspirin 81 mg due to a label mix-up where one bottle contained Acetaminophen 500 mg.
Buurma Farms is recalling fresh cilantro after a customer reported a positive Listeria monocytogenes test result from the Michigan Department of Agriculture.
Bethel Nutritional Consulting, Inc. is recalling Bethel 30 capsules because FDA analysis found undeclared sibutramine and phenolphthalein, making the product an unapproved new drug.
Fresenius Kabi is recalling 15,625 vials of Magnesium Sulfate Injection, USP, 50% due to the presence of glass particulate matter.
Toyota is recalling specific Lexus GS 350, IS 350, and IS 350C vehicles because engine bolts may loosen, potentially causing the engine to stop while driving.
Zimmer, Inc. is recalling 771 units of the Trabecular Metal Reverse Shoulder Glenosphere Distractor due to potential mechanical failure if used without proper lubrication.
Nexus Pharmaceuticals is recalling 46,185 vials of Benztropine Mesylate Injection due to the presence of glass delamination flakes.
Toyota is recalling 2006-2010 Highlander and 2006-2008 Lexus RX hybrids because a defective inverter component may cause the vehicle to stall unexpectedly while driving.
Clinical Specialties Compounding Pharmacy is recalling Avastin syringes due to sterility assurance issues and reports of eye infections.
Waldemar Link is recalling six trial stems for the MP Reconstruction Prosthesis because they were manufactured using the wrong design.
Megadyne Medical Products is recalling specific lots of E-Z Clean Disposable Laparoscopic Electrodes due to potential insulation breaches.
Hospira Inc. is recalling 72,300 vials of Diazepam Injection due to ineffective crimps that may compromise sterility.
Novocol is recalling two lots of Lidocaine 2% with Epinephrine 1:100,000 injection because the epinephrine component may be subpotent.
Waldemar Link is recalling 9 trial stems for the MP Reconstruction Prosthesis because they were manufactured using the wrong design. The units were distributed only in Tennessee.
Whole Foods Market is recalling Sour Cherry Crostata pies because egg wash is used in the product but is not listed on the ingredient list or allergen statement.