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
Launch Sequence Euphoria Capsules have been recalled because the product contains undeclared tadalafil, an unapproved active ingredient. The capsules were distributed nationwide in the USA and Canada.
Blazos Pie Shoppe is recalling 9-inch peanut butter cream pies possibly contaminated with Salmonella. The affected products with code dates 6/23 and 6/27 were distributed in Michigan.
Launch Sequence Capsules dietary supplement recalled for containing undeclared tadalafil, an FDA-approved pharmaceutical ingredient. The product was marketed without required drug approval.
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.
Volkswagen is recalling 1,216 2016 Audi and Volkswagen vehicles because the front passenger air bag may explode or deploy improperly, posing a risk of serious injury or death.
Blount Fine Foods is recalling Panera Bread at Home Southwest Corn Chowder due to undeclared wheat. The product poses a health risk to consumers with wheat allergies or celiac disease.
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.
FDA recalls Ortiga mas Ajo Rey dietary supplement sold nationwide due to undeclared diclofenac. Product marketed as supplement contains pharmaceutical ingredient not listed on label.
Ferrari is recalling various models from 2005-2022 because a defective brake fluid reservoir cap may cause a leak, leading to partial or total loss of brake function.
Spartan Fire is recalling 2020-2021 Metrostar and Gladiator fire trucks because a loose electrical connection may cause the load center to overheat and increase the risk of a fire.
E-One is recalling specific 2019-2022 fire trucks because a loose electrical connection may cause the load center to overheat, increasing fire risk.
Capacity of Texas is recalling 2021-2022 TJ 5000, 6500, and 9000 trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.
Shyft Group is recalling certain 2022-2023 Spartan RV Chassis vehicles due to improperly assembled steering gears that may fracture, causing loss of steering control. Owners should contact the manufacturer for free inspection and replacement.
Ember is recalling 2022 Overland series trailers because cracked LP gas fittings may cause a leak, increasing the risk of fire.
Lion Electric is recalling 2020-2022 Lion C school buses because the parking brake may fail if not properly adjusted, increasing crash risk.
Ford is recalling certain 2022 F-53 and F-59 motorhome and commercial chassis vehicles because the steering wheel attachment bolt may loosen and separate. This could result in loss of steering control and increased crash risk.
Jaguar Land Rover is recalling certain 2022-2023 Land Rover Defender and other models due to defective front seat belt pretensioners that may fail to properly restrain occupants in a crash, increasing injury risk.
Cheetah Chassis is recalling 2023 trailers because twist lock handles may separate, creating a road hazard or unsecuring containers.
Bryant Ranch Prepack has recalled Morphine Sulfate extended-release tablets due to a label mix-up where bottles may contain the wrong strength. Contact your pharmacy to verify your correct dose.
Morphine Sulfate extended-release tablets (30 mg) distributed in Alabama were recalled due to a critical label mix-up where bottles labeled as 60 mg contain 30 mg, and bottles labeled as 30 mg may contain 60 mg.
J & M Foods is recalling Favorite Day Lavender Shortbread Cookie Bites for undeclared egg and soy lecithin. Consumers with allergies to these ingredients should not consume the product.
Natreve Vegan Protein Powder (Lot# 46359 and 46360) is recalled nationwide due to an undeclared milk allergen.
Zeltiq Aesthetics is voluntarily recalling CoolCurve+ ZELTIQ Vacuum Applicators due to increased reports of Paradoxical Hyperplasia during 2019–2021, an adverse event involving abnormal fat growth at treatment sites.
MSI Express Inc. is recalling Knorr Curry Chicken and Rice Soup Mix because it contains undeclared milk, a known allergen.
Wawa cold brew coffee pints are being recalled due to undeclared peanuts. Approximately 1,000 units were distributed in Delaware, Florida, Maryland, New Jersey, Pennsylvania, Virginia, and Washington DC.