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
Atrium Medical is recalling ADVANTA VXT vascular grafts worldwide after reports of the slider swivel rod separating from the swivel core with a notable gap between components.
Atrium Medical is recalling ADVANTA VXT vascular grafts worldwide due to complaints of the swivel rod separating from the core, which could compromise device function during medical procedures.
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. The recall affects 53,308 units distributed worldwide.
Atrium Medical's ADVANTA VXT vascular grafts are recalled due to reported separation of the slider component from the swivel core. Over 53,000 units worldwide may be affected.
Stryker Neurovascular is recalling certain lots of Synchro2 Guidewires due to PTFE coating damage caused by backloading through an introducer accessory with manufacturing variations. Affected users should discontinue the backloading technique.
Panera Kitchen Sink Cookie dough pucks from Rise Baking Company are being recalled due to potential Salmonella contamination. The recall covers 29,019 cases distributed across 20 U.S. states.
El Mirasol, Inc. is recalling Tortilla de Harina flour tortillas in Florida due to undeclared wheat allergen. Consumers with wheat allergies should not consume this product.
Rise Baking Company is recalling Cowboy Cookie dough pucks distributed across 20 states due to potential Salmonella contamination. Affected cases are identified by code 4117N1.
Atrium Medical Corporation recalled FLIXENE vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units are affected worldwide.
Happy Farms cream cheese spreads sold at Aldi were recalled due to potential Salmonella contamination affecting 835,721 units distributed across 19 states and Puerto Rico.
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the slider rod from the swivel core, with a gap between components. Approximately 53,308 units are affected globally.
Atrium Medical recalls FLIXENE vascular grafts due to complaints of the Slider GDS Swivel Rod separating from the Swivel Core. Component separation in implanted vascular grafts could compromise device function.
The Arial mobile application experiences frequent restarts on iOS 17.4 and 17.5, causing alert overload, communication failures, and offline status in healthcare facilities.
WAVi Co. is recalling 281 units of the WAVi Research EEG Desktop System following an FDA-issued Warning Letter. The company requested the return of components due to closure of their research study.
Della Fattoria, LLC is recalling 115 loaves of Della Fattoria Seeded Wheat Bread sold in California because the product contains sesame seeds but sesame is not declared on the label.
Atrium Medical Corporation is recalling the Advanta VXT vascular graft due to reports of the swivel rod separating from the swivel core. The recall affects approximately 53,308 units distributed in the United States and worldwide.
Eveland is recalling 2024 Scamp trailers because a cooktop circuit board may overheat, increasing the risk of fire. Dealers will repair the issue free of charge.
Thor Motor Coach is recalling 2025 Tranquility and Sanctuary motorhomes because an incorrect circuit breaker can cause wiring to overheat and increase fire risk.
New Flyer is recalling 2023 XD35, XD40, and XD60 buses because fuel filter hoses may separate, causing leaks or engine stalls.
Thor Motor Coach is recalling certain 2024-2025 Luminate and Indigo motorhomes because the heat shield protecting the propane tank from engine exhaust may be too short, risking tank overheating and fire.
Waymo is recalling 672 5th Generation Automated Driving Systems due to a software defect that could prevent the system from avoiding poles or similar objects.
Volkswagen is recalling 2024 Audi Q8 E-Tron vehicles because an over-tightened brake line connection may leak fluid, reducing braking ability and increasing crash risk.
Dana Incorporated is recalling D-Series and E-Series steer axles and replacement tie rod assemblies because incorrectly heat-treated ball studs may break, potentially causing loss of steering control.
USDA FSIS issued a public health alert for Bistro Grande Southwestern Style salad bowls containing undeclared wheat and fish allergens.
Volvo Trucks North America is recalling 2025 VN trucks because improperly heat-treated tie rod assemblies may fail, causing sudden loss of steering control.