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 deaths or serious injuries are reported, 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
Nissan is recalling 2020-2021 Sentra vehicles because the left or right tie rod may be bent. A bent tie rod can break, causing loss of steering control and increasing crash risk.
General Motors recalls certain 2021 Chevrolet Tahoe and related vehicles due to a power steering software issue that may cause loss of steering assist, increasing crash risk.
Heartland Recreational Vehicles is recalling certain 2021 Mallard and other trailers because LP gas lines on outside cooktops may not have been tightened properly, creating a risk of gas leaks and fire.
Certain 2020-2021 Land Rover Discovery vehicles have a loose battery ground contact causing electrical failure and potential vehicle shutdown while driving. Dealers will replace the ground stud at no cost.
Avid Medical is recalling 160 fistula care kits due to potential contamination from Aspergillus penicillioides fungal growth in a component applicator. The contamination could breach the kit's package integrity and affect other sterile components.
Avid Medical is recalling 130 Adult Chest Tube Trays due to potential contamination from mold growth in a component. The BD ChloraPrep applicator may grow Aspergillus penicillioides, which could breach package integrity and contaminate other kit components.
DeRoyal Industries is recalling 66 heart catheterization procedure packs due to mislabeling of anesthetic contents. The packs contain 0.5% Bupivacaine but are labeled as containing 1% Lidocaine, creating a medication error risk during surgery.
Hy-Vee is recalling Chicken Street Taco kits because the chipotle crema component contains undeclared egg, a major food allergen. The product was distributed to Hy-Vee stores across multiple states.
BC Foods is recalling Celery Stalk and Leaf Dice due to an ingredient testing positive for Salmonella. The product was distributed to food manufacturers and distributors across eight states.
BCFoods, Inc. is recalling certain BC Foods AD Celery Stalk products because an ingredient tested positive for Salmonella. The affected products are sold in bulk fiber cartons to food service and manufacturing customers.
Gilster-Mary Lee Corp. is recalling Organic Microwave Butter Popcorn because butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes, resulting in undeclared milk in the product. The recall affects 413 cases distributed to multiple states.
Avid Medical is recalling 720 Fistula On-Off Kits due to potential fungal contamination that may compromise package integrity. The BD ChloraPrep applicator component may develop Aspergillus penicillioides, which could contaminate other kit components.
Avid Medical is recalling medical dialysis access kits due to potential fungal growth in an applicator component that may compromise the package seal and contaminate other components. Approximately 560 kits distributed nationwide are affected.
Innova Medical Group recalled COVID-19 self-test kits distributed to customers outside of clinical investigation requirements. About 1,206 tests in 402 boxes were distributed across the U.S., Canada, India, and the United Kingdom.
Rainfield Marketing Group is recalling 150g packages of Enoki Mushroom (UPC 085412004020) because samples tested positive for Listeria monocytogenes. The product was distributed to California, Texas, and Maryland.
Innova Medical Group is recalling COVID-19 self-test kits distributed to customers outside an authorized clinical investigation. The recall affects 370 boxes of tests distributed nationwide and internationally.
DeRoyal is recalling surgical procedure packs due to mislabeling. The product contains 0.5% Bupivacaine but is labeled as 1% Lidocaine, creating a medication identification error.
INNOVA Medical Group is recalling SARS-CoV-2 antigen rapid test kits distributed to customers not enrolled in an authorized clinical investigation.
DeRoyal Angio Cath Removal Tray contains mislabeled anesthetic; the label indicates 1% Lidocaine but the tray actually contains 0.5% Bupivacaine. This FDA Class I recall affects 60 trays distributed in MS, VA, LA, and NY.
Smiths Medical recalls 1,432,200 Jelco insulin syringes with skewed graduation markings that could lead to incorrect dosing. Specific lot numbers are affected.
365 Everyday Value Whey Protein Powder was mistakenly packaged with Soy Protein Powder. The affected canisters were distributed nationwide and may pose a risk to consumers with soy allergies.
Sun Hong Foods is recalling Seafood Mushroom (5.3 oz packages) distributed to California, Texas, Washington, Illinois, Florida, and New York due to potential Listeria monocytogenes contamination identified in product testing by the California Department of Public Health.
RayStation radiation therapy treatment planning software versions 6 through 10A contain defects that may cause misleading dose evaluations and contouring errors. Healthcare facilities should verify treatment plans and contact the manufacturer for guidance.
Cove Appliance is recalling about 42,000 built-in dishwashers because the heating element can fail to shut off and overheat, creating a fire hazard. The company has received five reports of burning smells, flames, and smoking inside the dishwashers, though no injuries have been reported.
CooperSurgical has recalled its Wallach Loop Electrodes (Lot 274420) due to incorrect packaging. Packages labeled as Square Electrodes contained Round Electrodes instead, creating a risk of improper device use in surgical procedures.