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
Nova Bus is recalling 2009-2021 LFS and LFS Artic transit buses because non-standard color auxiliary lights may distract other drivers and increase crash risk.
Heritage Pharmaceuticals' desmopressin acetate tablets (0.2mg) have been recalled nationwide due to subpotency. The voluntary recall affects 13,805 bottles; no illnesses have been reported.
Greer Laboratories recalled a hypersensitivity pneumonitis test kit (102 units, Lot 389592) after stability testing revealed decreased reactivity that could cause false-negative results. The issue was discovered in October 2021.
Amy's Kitchen is recalling Gluten Free Bean and Cheese Burritos (Lot 30H0922, best before 08/2024) due to potential plastic pieces in the product. Approximately 5,134 cases were distributed to 18 U.S. states.
Noven Pharmaceuticals recalls 3,977 boxes of Daytrana methylphenidate transdermal patches nationwide due to defective adhesive properties in lot 91316. Affected patches may fail to adhere properly or deliver medication inconsistently.
Coolhaus Dairy Free Cookie Dough Lyfe frozen dessert sandwiches recalled due to coliform detected in lab samples. Product distributed to select retailers in Texas, Maryland, Colorado, and California.
Cytocell Ltd. recalls CytoCell BCL11B Proximal probe used in T-cell malignancy testing (lot RD22/230/10). The package insert contains an incorrect chromosome map that doesn't match the probe design.
Busse Hospital Disposables is recalling 40 cases of Busse Spine Injection Trays containing 3M Steri-Drape Surgical Drapes distributed in Texas due to a defective adhesive liner that is difficult to remove without damaging the product.
A. MENARINI diagnostics hemoglobin A1c control materials (Lot 12161) are producing incorrect results that cause analyzer errors and prevent diagnostic testing. Facilities using this lot should discontinue use and contact the manufacturer.
Primus Corporation recalls Trinity Biotech HbA1c Control Kits because Control Level I material produces out-of-range results that cause analyzer malfunction and testing delays, potentially delaying patient results.
Volkswagen Group of America is recalling 2023 Audi S3, RS3, and A3 vehicles because the B-pillar safety label is missing weight capacity information.
Acella Pharmaceuticals is recalling Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads because testing found the drug out of specification for potency at shelf-life expiration. 528 cartons distributed nationwide are affected.
Dr. Reddy's Laboratories is recalling Allergy Relief D extended-release tablets distributed nationwide by Walmart due to failed dissolution specifications. No illnesses or injuries have been reported.
3M is recalling Steri-Drape Surgical Drapes because the liner on the adhesive component is difficult to remove without damaging the product, potentially rendering it unusable.
Cytocell Ltd. is recalling a diagnostic reagent due to an error in the chromomap on the package insert. The nucleotide locations in the text are correct, but the chromosome map was created using incorrect coordinates.
Kia is recalling 2020 Niro EV vehicles because a coolant leak in the Electric Power Control Unit may cause loss of drive power, increasing crash risk.
Porsche is recalling 2022-2023 911 vehicles because the dashboard console may break during air bag deployment, increasing injury risk.
Hino is recalling 970 specific 2022-2023 models because a fuel tube may restrict fuel flow, potentially causing engine stalls and increasing crash risk.
KTM is recalling 2020-2022 1290 Super Duke R motorcycles because the main wiring harness may be misrouted or missing parts, potentially causing an electrical short-circuit and engine stall.
Volvo Trucks is recalling certain 2022-2023 VNL vehicles because excessively tightened air tank bracket fasteners may break, allowing the air tank to detach and become a road hazard.
Tesla is recalling 2023 Model Y vehicles because front suspension fasteners may not be properly attached, which could cause instability and increase crash risk.
Kraft Heinz is recalling approximately 2,400 pounds of Oscar Mayer Ham and Cheese Loaf products due to possible cross-contamination from under-processed items.
LDV is recalling 2013 and 2019-2022 Emergency Response vehicles due to improperly connected propane tank service valves that may cause leaks.
Continental Tire is recalling specific 4x4 Contact, PureContact LS, and TerrainContact H/T tires because overcuring may cause sidewall breaks or tread separation, increasing crash risk.
USDA FSIS issued a public health alert for ground beef sold at La Michoacana Meat Market in Greenville, Texas, after testing positive for E. coli O157:H7.