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
Blue Bird is recalling 2018-2023 Vision buses with specific LPG systems because fuel lines may corrode and leak, increasing fire risk.
Blue Bird is recalling 2017-2023 Vision school buses with specific LPG conversion systems because fuel line corrosion may cause leaks and fire.
Mylan Pharmaceuticals is recalling Insulin Glargine prefilled pens (lot BF21002895) distributed nationwide because some pens lack labels, which could prevent patients from properly identifying and administering the medication.
Baxter Healthcare's ABACUS TPN calculation software poses a potential risk of medication error. The FDA issued a Class I recall; healthcare providers should contact the manufacturer for guidance.
Fuchs North America is recalling Za'atar Seasoning (lot 252491) because an oregano sub-ingredient tested positive for Salmonella. The product was distributed to one commercial buyer.
Pfizer is recalling 54,000 vials of Propofol Injectable Emulsion (Lot DX9067) due to presence of particulate matter identified as a beetle. No illnesses or injuries have been reported.
BD Intraosseous Needle Kits have been recalled due to mechanical failures that could prevent emergency vascular access. Affected units nationwide and in Canada may experience stylet removal problems, safety mechanism failures, or driver malfunction.
Volkswagen Group of America is recalling one 2022 Audi SQ5 Sportback because the rear lid connections may be improper, potentially reducing crash protection.
Kalmar is recalling 2021-2022 Ottawa T2 terminal tractors because incorrectly assembled steering gears may fracture, causing loss of steering control and increasing crash risk.
Valor Compounding Pharmacy is recalling Nifedipine WSP 0.2% Ointment due to potency variability. Some batches may be subpotent or superpotent, affecting safety and efficacy.
Integra LifeSciences is recalling CereLink ICP Monitors due to electrical interference causing intracranial pressure readings to drift out of range. Affected devices may display an error message indicating sensor or extension cable failure.
Delco Trailers is recalling 2021-2022 C, D, and F-Series trailers because a defective axle weld may crack or separate, increasing crash risk.
Xtreme Outdoors is recalling 2021-2022 Little Guy Max and Mini Max travel trailers with improperly tightened axle bolts that could cause axle detachment and increase crash risk.
Forest River is recalling certain 2022 Flagstaff and 2022-2023 Rockwood tent campers due to improperly installed axles that can reduce brake function. Owners should contact their dealer for free inspection and repair.
E-One is recalling 2021-2022 Typhoon N and Cyclone N vehicles because incorrectly assembled steering gears may fracture, potentially causing loss of steering control.
Conagra Brands is recalling P.F. Chang's Home Menu Beef & Broccoli because the product contains egg, an undeclared allergen. No illnesses have been reported.
Daimler Trucks North America is recalling 2023 Thomas Built Saf-T-Liner HDX and C2 school buses because the engine control module may short-circuit, causing unexpected engine shutdown.
Nissan is recalling 2017-2019 Rogue Hybrid vehicles because the hydraulic brake booster may overheat, causing a loss of power brake assist and increasing crash risk.
Eldorado is recalling 2021-2022 Axess vehicles because incorrectly assembled steering gears may fracture, causing loss of steering control and increasing crash risk.
Daikin Comfort Technologies is recalling about 298,300 evaporator coil drain pans that can overheat, melt, and deform, creating a fire hazard. The company has received 26 fire reports, with no injuries reported.
Gillig is recalling 184 Low Floor vehicles from 2019-2022 because battery packs may leak coolant and short circuit, increasing the risk of fire.
USDA FSIS is recalling approximately 19,275 pounds of frozen meat pizzas from Danny's Sub and Pizza because they were produced without federal inspection.
Amazon is recalling Artri King herbal supplement tablets nationwide due to FDA laboratory findings of undeclared diclofenac, a pharmaceutical medication not listed on the label. The product was marketed without FDA approval.
Launch Sequence Aphrodisia Capsules contain undeclared tadalafil, making them an unapproved drug. The recall involves 500 4-count tins distributed nationwide in the USA and Canada.
The FDA is recalling Artri Ajo King tablets nationwide after finding they contain undeclared diclofenac, a prescription anti-inflammatory drug. Affected bottles (lot LTARTKNGOMG30220, expiring December 2025) were sold on Amazon.