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
Autocar is recalling 2021-2023 Xpeditor vehicles because the steering column shaft pinch bolt may be improperly secured and bind, causing sudden loss of steering and increasing crash risk.
Ford is recalling certain 2023 E-450 vehicles because rear axle rotor bolts may be improperly tightened, risking wheel separation and increasing crash risk. Dealers will replace affected assemblies at no charge.
Shyft Group is recalling certain 2021-2023 Spartan K2 RV Chassis due to undersized air brake supply reservoirs that may fail to provide sufficient air for proper brake operation, increasing crash risk.
Approximately 620,000 COVID-19 rapid test devices were distributed in the U.S. without FDA Emergency Use Authorization or approval. Consumers should not use these unauthorized test kits.
Albertsons Companies LLC is recalling Ready Meals Shrimp Cooked with Cocktail Sauce due to undeclared fish (anchovy) allergen. The product was distributed to Oregon and Washington stores.
About 22,000 Ancheer e-bikes with lithium-ion batteries are being recalled because the batteries can ignite, explode, or spark, causing fire and burn injuries. Consumers should stop using the recalled bikes immediately and contact Ancheer for a free replacement battery and mount.
U-Line is recalling about 90 Outdoor Series 24-inch built-in convertible freezers that can overheat and pose a fire hazard. U-Line has received three reports of freezer fires with no injuries reported.
BRP is recalling certain 2022 Ski-Doo snowmobiles with 850 E-TEC engines due to a loose fuel injector hose retainer screw that can cause fuel leaks and fires. The company has received five fuel-leak reports, resulting in two fires.
Arcade Industries candy corn sold at Shapiro Produce stores in Massachusetts and Connecticut is recalled due to undeclared egg allergen. People with egg allergies risk allergic reaction.
Renaissance Food Group is recalling its Small Ranch Tray with Dip due to positive test results for Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Large Mild Salsa (13 oz) due to positive Listeria monocytogenes test results. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Mushroom Stir Fry Blend after testing detected Listeria monocytogenes in the finished product. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling 3 Skewer Veggie Kabobs due to confirmed Listeria monocytogenes contamination. Products were distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Mexican Style Layered Bean Dip (1.25 lb) distributed in Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes.
Philips Respironics Amara View Full-Face Mask lacks critical safety warnings about magnetic components for patients with implantable medical devices. The Class I recall affects 5.6 million units worldwide.
Kenover Marketing Corp. is recalling Mighty Sesame Organic Tahini over potential Salmonella contamination. Approximately 13,766 units were distributed to stores across 20 states.
Philips Respironics is recalling Wisp and Wisp Youth nasal masks because they lack warnings about magnetic components that could interfere with implanted medical devices or cause eye injuries from metallic splinters.
Renaissance Food Group is recalling Hamburger Fixin's (10 oz units) distributed in Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in the finished product.
Renaissance Food Group is recalling Medium Hatch Salsa (13 oz units) because positive test results detected Listeria monocytogenes in the finished product. The affected salsa was distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Tri-Pepper Blend (7 oz units) due to positive test results for Listeria monocytogenes. All products manufactured with the same components are included in the recall.
Renaissance Food Group is recalling 106 units of Seasoned Squash Onion & Dill due to detection of Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Vegetable Bowl products because testing found Listeria monocytogenes contamination. The products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Steak Topper seasoning (7.5 oz units) due to positive test results for Listeria monocytogenes. The affected product was distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Fiesta Corn (10 oz) after positive test results confirmed Listeria monocytogenes in the finished product. All products made with the same components are affected.
Antigua Farmacista Hand Sanitizer Ocean Citron (473 mL bottles) is being recalled because the product was found to contain benzene. The affected lot was distributed in Florida and Washington only.