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
G & M Co. is recalling approximately 3,586 pounds of beef products that may be contaminated with E. coli O157:H7. The products were shipped to retail locations in New Jersey and New York.
Spartan is recalling 2017 Gladiator and K3 motorhome chassis due to a potential electrical short in the engine control module that could cause the engine to stall.
Triumph is recalling aftermarket adjustable brake levers for specific 2016-2017 motorcycles because they may contact the handlebar, preventing maximum braking force.
Asian Jade Customs Brokerage is recalling approximately 762 pounds of imported dried pork sausage that was not inspected at the U.S. point of entry.
Vermeer is recalling 2014-2016 TG5000 trailers because incorrect pushrod lengths may cause parking brakes to engage unintentionally, increasing crash risk.
Nissan is recalling 2014-2016 Infiniti Q50 and Q50 Hybrid vehicles because a steering system error may alter responsiveness and increase crash risk.
McNeilus is recalling 19 model year 2016 Bridgemaster V Concrete Mixers because bridge axle tube sleeves may crack, potentially causing the axle to detach and increasing crash risk.
Hendrickson is recalling specific bridge axles manufactured in late 2015 and early 2016 because tube sleeves may crack, potentially causing the axle to detach from the vehicle.
Maserati is recalling 2014 Quattroporte and Ghibli vehicles because the gear indicator may mislead drivers about the transmission position, creating a risk of injury when exiting.
PACCAR is recalling 2017 Kenworth and Peterbilt trucks because a defective engine control module may cause the engine to stall without warning, increasing crash risk.
Vermeer is recalling 2014-2016 TG5000 Tub Grinder trailers because incorrectly installed spherical washers may cause the kingpin to detach, increasing crash risk.
Honda is recalling specific 2015-2016 Odyssey, Acura MDX, and Pilot vehicles because fuel tank welds may separate, causing a leak that could lead to a fire.
Daimler Trucks is recalling 2008-2009 Sterling Bullet 4500 and 5500 chassis cabs because passenger air bag inflators may rupture, posing a risk of serious injury or death.
Patel Shippers Inc is recalling fresh long chili peppers imported from the Dominican Republic because they tested positive for Salmonella.
The Kroger Co is recalling Roasted & Salted Sunflower Kernels due to potential Listeria monocytogenes contamination.
The Kroger Co is recalling Salted Sunflower Kernels because the supplier notified the firm that the product may be contaminated with Listeria monocytogenes.
The Kroger Co is recalling Cranberry Delight Trail Mix because it may be contaminated with Listeria monocytogenes.
Integra LifeSciences is recalling 2,487 MicroFrance electrosurgical instruments due to reports of unintended patient or operator burns and electric shock.
World's Choice Products is recalling Supreme Elixir 32oz. bottles due to undeclared whey protein containing milk and soy lecithin.
Akorn, Inc. is recalling specific lots of Sulfacetamide Sodium Ophthalmic Solution because they failed antimicrobial effectiveness testing, raising concerns about sterility.
Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.
Baptist Health Medical Towers Pharmacy is recalling seven bags of TPN 1 (amino acid 20%) in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 88 bags of Vancomycin 1500 mg in 270 mL 0.9% NS due to a lack of sterility assurance.
FDA is recalling Curity All Purpose Sponges due to compromised sterility from a barrier breach. The recall affects units distributed in the US and 20 other countries.
Frank L Harter & Sons Inc. is recalling 548 cases of 5 lb pasta salad containers because the labels failed to list milk and soy as ingredients.