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
Gallo Meats LLC is recalling approximately 82 pounds of sausage, beef, and lamb products produced without federal inspection. The hot Italian sausage may also contain undeclared allergens.
Bunge's Meats is recalling pork sausage products made with water that failed EPA drinking water standards due to Coliform bacteria.
Tucson Tamale Wholesale Company is recalling 915 pounds of beef tamales because the meat was produced without federal inspection. No illnesses have been reported.
Polaris is recalling about 42,500 model year 2014 Ranger 900 vehicles because a heat shield can fall off, creating fire and burn risks.
GE Appliances is recalling about 222,000 Profile top-loading clothes washers because an electrical component can overheat and cause a fire.
Samsung is recalling Galaxy Note7 smartphones sold before September 15, 2016, because the lithium-ion battery can overheat and catch fire, posing a burn hazard.
Chrysler is recalling specific 2010-2014 models because a module may short circuit, preventing airbags and seat belt pretensioners from deploying in a crash.
Schulze & Burch Biscuit Co is recalling Aldi's Millville protein chew bars because a supplier reported Listeria monocytogenes in an ingredient.
Schulze & Burch Biscuit Co is recalling Aldi's Millville dark chocolate peanut butter protein chew bars because a supplier reported Listeria monocytogenes in an ingredient.
Amerisource Health Services is recalling 126 cartons of amphetamine extended-release capsules due to unit dose mispackaging where blister cavities may contain multiple capsules.
MicroPort Orthopedics is recalling Advance II Modular Tibial Bases due to a higher than expected revision rate caused by component loosening.
Allergy Laboratories is recalling Ephedrine Sulfate Injection vials because an FDA inspection raised concerns about product sterility.
Amerisource Health Services is recalling 115 cartons of 25 mg amphetamine extended-release capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
MicroPort Orthopedics is recalling 77 Advance II Modular Tibial Bases because they are experiencing higher than expected revision rates due to component loosening.
MicroPort Orthopedics is recalling Advance II Modular Tibial Bases due to a higher than expected revision rate caused by component loosening.
MicroPort Orthopedics is recalling Advance II Modular Tibial Bases due to a higher than expected revision rate caused by component loosening.
Amerisource Health Services is recalling 2,276 cartons of 10 mg amphetamine tablets because blister cavities may contain more than one tablet.
Aribex Inc is recalling 16,871 NOMAD Pro2 X-Ray systems because internal lithium-ion batteries may short-circuit, causing overheating, smoke, or ignition.
ConAgra Frozen Foods is recalling PF Chang's Home Menu Shrimp Lo Mein because metal fragments were found in a raw ingredient used during manufacturing.
MicroPort Orthopedics is recalling 47 units of Advance II Modular Tibial Bases due to a higher than expected revision rate caused by component loosening.
Aribex Inc is recalling NOMAD Pro X-Ray systems because internal lithium-ion batteries may short-circuit, causing overheating, melting, smoking, or ignition.
Teva North America is voluntarily recalling 92,480 containers of Linezolid Injection 600 mg/300 mL due to CGMP deviations. The recall covers products distributed nationwide and in Puerto Rico.
MicroPort Orthopedics is recalling 38 units of Advance II Modular Tibial Bases because they are experiencing a higher than expected revision rate due to component loosening.
MicroPort Orthopedics is recalling Advance II Modular Tibial Bases due to a higher than expected revision rate caused by component loosening.
MicroPort Orthopedics is recalling Advance II Modular Tibial Bases due to a higher than expected revision rate caused by component loosening.