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
Alliance RV is recalling 2025-2027 Valor and 2026-2027 Delta recreational trailers because a power cord fuse may not provide adequate circuit protection, increasing fire risk.
Forest River is recalling 2026-2027 Cedar Creek recreational trailers because a slide switch may lack proper overcurrent protection, creating a fire risk.
Porsche is recalling 548 specific 2024 models because a center lock wheel bolt may fracture, causing the wheel to detach and increasing crash risk.
Wabash is recalling 2027 Van Trailers because incorrect wheel bearing lubricant may cause wheel lock-up, increasing the risk of a crash.
3M is recalling Scotch thermal laminators because they can overheat and catch fire. Consumers should stop using the devices and contact 3M for a refund.
HatsanUSA is recalling Blitz and Blitz 777 air rifles because they can fire unexpectedly, posing a risk of serious injury or death.
Volvo Trucks is recalling specific replacement sleeper cabs for VNL660 and VNL860 models because loose or missing structural bolts may reduce occupant protection during a crash.
Papablic is recalling convertible bedside sleepers with play yard extensions due to risks of serious injury or death from entrapment, suffocation, and falls.
Shyft Group is recalling 2024-2027 Spartan RV Chassis K2 vehicles because remote fuel filter hoses may separate, causing fuel leaks and engine stalls.
usOpal is recalling Xalirium Adult Portable Bed Rails because they violate safety standards, posing risks of entrapment, asphyxiation, and falls.
Volvo Trucks North America is recalling 2025-2026 VNL (4) trucks because loose or missing structural bolts in the cab may reduce occupant protection during a crash.
Primark is recalling 101 Dalmatians Faux Leather Coin Purses because they contain higher phthalate levels, posing a risk of ingestion by young children.
Jaguar Land Rover is recalling 2022-2026 Range Rover vehicles because water may not drain from the rearview camera, potentially causing image failure and increasing crash risk.
Loving Thyself Rocks is recalling about 600 crystal glass cups because loose crystal chips can break, posing a risk of serious injury from ingestion and laceration.
Prevost is recalling certain buses because the entrance door is missing the emergency exit operating instruction label, which may delay evacuation during an emergency.
Berlin Seeds is recalling alfalfa sprouting seeds due to potential E. coli and/or Salmonella contamination. The product was sold in Ohio and nationwide online.
Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 26/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
LEASA Living Alfalfa Sprouts are being recalled because the seeds may have been contaminated with E. coli. The product was distributed in Florida and New Hampshire.
K.C. Pharmaceuticals is recalling 163,008 cartons of Leader Ultra Lubricating Eye Drops due to a lack of assurance of sterility. The product was distributed nationwide under multiple brand names.
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used may have compromised the product's sterility.
Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable products due to a lack of assurance of sterility related to formulation and processing equipment.
Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 85/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
K.C. Pharmaceuticals is recalling 1,327,248 cartons of dry eye relief eye drops due to a lack of assurance of sterility. The products were distributed nationwide under multiple brand names.
Steris is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low, potentially causing false results in steam sterilization monitoring.
Apothecary Pharma LLC is recalling 22 vials of Tirzepatide Injection due to a lack of assurance of sterility. The affected product was distributed nationwide.