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
Keystone RV Company is recalling 2019 Montana recreational trailers because defective axle welds could cause the wheel assembly to detach, increasing crash risk.
Mercedes-Benz is recalling specific 2015-2019 models because a steering rack locknut may break, causing the steering to stick and increasing crash risk.
Sprout Creek Farm, Inc. is recalling Margie Cheese wheels contaminated with Listeria monocytogenes. The recall affects one-pound wheels sold in New York.
Bazzini LLC is recalling specific lots of roasted and salted in-shell pistachios because the product tested positive for Salmonella.
Bazzini LLC is recalling 25 lb boxes of roasted and salted in-shell pistachios because the product tested positive for Salmonella.
Sciegen Pharmaceuticals is recalling Irbesartan 300mg tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Bazzini LLC is recalling specific lots of roasted and salted in-shell pistachios because the product tested positive for Salmonella.
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, 75 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Altec is recalling 2017 AT37, AT41, and AT48 aerial devices because loose or missing fasteners may cause the pedestal to separate, increasing injury risk.
Confections by Michael Recchiuti is recalling specific lots of Recchiuti Feve Dark Chocolate because FDA analysis found high levels of milk protein in the dairy-free product.
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, 150 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Ford is recalling 2016-2018 Focus vehicles with 1.0L engines and manual transmissions because a clutch fracture could cause a fluid leak and fire risk.
Smiths Medical is recalling 10,440 Irrisept OR bottle assemblies because leaking containers may compromise sterility, posing an infection risk.
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, USP, 300 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Elaboraciones Felo, Inc. is recalling Pizza Turnovers because the products failed to declare wheat and soy allergens. The recall covers 7,011 cases distributed in Puerto Rico.
Confections by Michael Recchiuti is recalling specific lots of Bittersweet Dark Chocolate because FDA analysis found high levels of milk protein.
Golden State Medical Supply is recalling 12,502 bottles of Irbesartan 300 mg tablets because FDA testing found the impurity N-nitrosodiethylamine (NDEA).
TSE Brakes is recalling specific Air Brake Actuators because mounting washers may fracture, potentially reducing braking ability and increasing crash risk.
Sedecal S.A. is recalling 145 NOVA FA DR diagnostic radiography systems because installation or maintenance issues could cause support cables to break, leading to equipment falling.
Golden State Medical Supply Inc. is recalling 2,439 bottles of Irbesartan 75 mg tablets because FDA testing confirmed the presence of the impurity N-nitrosodiethylamine (NDEA).
Porsche is recalling 2018 Panamera Hybrid models because front brake lines may corrode, potentially reducing braking performance and increasing crash risk.
Sciegen Pharmaceuticals is recalling Westminister Irbesartan Tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Bazzini LLC is recalling 4,000 lbs of roasted and salted in-shell pistachios because the product tested positive for Salmonella.
Keystone RV Company is recalling certain 2019 recreational trailers because the inner axle hub bearings may not have been sufficiently greased, which could cause overheating, hub failure, and increased crash risk.
Golden State Medical Supply is recalling Irbesartan 150 mg tablets because FDA testing found the impurity N-nitrosodiethylamine (NDEA).