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
AURIS HEALTH INC is recalling approximately 110 units of the Monarch Platform bronchoscopy surgical device due to a software defect that can flip the displayed image during procedures. No injuries have been reported.
Integra LifeSciences recalled the Integra Cranial Access Kit (160 units) due to a defect in the outer packaging that can split and compromise device sterility, creating an infection risk for neurosurgical procedures.
Stryker is recalling ProCuity patient beds (model 3009) for missing required electrical safety test documentation, creating a risk of electrical shock or tissue burn.
Stryker is recalling ProCurity bed series (model 3009) due to missing electrical safety test values that could pose risk of electrical shock or tissue burn. Affected units were distributed nationwide and internationally.
BAPS Shayona is recalling its Anjir Roll sweet rolls (12 oz) for containing undeclared Yellow #5 food coloring. The product was distributed to Alabama, Florida, Georgia, North Carolina, South Carolina, and Tennessee.
BAPS Shayona is recalling Kesar Penda Ricotta fudge discs because they contain undeclared soy and Yellow #5 & #6 dyes. The product was distributed to six Southern states.
Garden of Life RM-10 mushroom supplement recalled due to undeclared soy, a common allergen. The recall affects 15,119 bottles distributed domestically and internationally; consumers with soy allergies should not use these products.
Garden of Life FYI ULTRA Joint & Cartilage Formula dietary supplement recalled due to undeclared soy. Consumers with soy allergies should not use affected bottles.
Elekta radiation therapy accelerators may experience uncontrolled detector arm extension due to an incorrectly set microswitch in the middle arm. The issue affects 315 units worldwide.
Heartware recalls HVAD ventricular assist pump instructions to clarify controller fault alarm conditions and component useful life expectations.
Wilson-Cook Medical is recalling 157 Quantum TTC Biliary Balloon Dilator devices due to a design defect that may cause balloon detachment during use, potentially requiring emergency retrieval.
Great Dane is recalling 2024 Champion trailers because improperly tightened axle spindle nuts could allow wheels to detach, increasing crash risk.
Tesla is recalling 2.03 million 2012-2023 Model S/X/3/Y vehicles with Autosteer due to insufficient control prominence that may allow driver misuse and crash risk. A free OTA software update will be provided.
Mazda is recalling 2004-2006 B-Series trucks because previously replaced front passenger air bag inflators may have been installed incorrectly, potentially preventing proper inflation during a crash.
REV Recreation Group is recalling 2016-2023 American Coach American Eagle motorhomes because turbulence may loosen or break the rear air deflector mounting bracket hardware.
Harley-Davidson is recalling certain 2023 FLHXSE motorcycles due to an engine control module software defect that may cause loss of control at high speeds, increasing crash risk.
Mercedes-Benz is recalling 2021-2022 GLE 350 and GLE 450 vehicles because a 12-volt ground connection may overheat, increasing the risk of a fire.
Forest River is recalling 2024 XLR Boost toy haulers because taillights may be insufficiently reflective, reducing visibility and increasing crash risk.
Wayne Farms is recalling approximately 1,377 pounds of ready-to-eat chicken breast products that may be undercooked. The recall was initiated after a customer complaint regarding product appearance.
Pierce is recalling 2019-2023 Arrow XT, Enforcer, and Velocity tower trucks because a wiring harness may not be secured, risking basket tipping and injury.
XpressGoods is recalling colorful neodymium magnetic balls that exceed federal safety limits for toy magnets. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.
Keystone RV is recalling 2021-2022 Dutchmen Coleman travel trailers with suspension springs rated at 4400 pounds instead of 5100 pounds. The underrated springs can become overloaded, increasing crash risk.
Volvo is recalling 2015-2024 XC90 vehicles because second-row seat belt buckle bolts may not be tightened properly, increasing injury risk in a crash.
Segway Powersports is recalling about 1,100 2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles because the ignition coil can fail, allowing fuel to enter the exhaust pipe and ignite, creating a fire hazard. One vehicle fire with property damage has been reported.
Security Equipment Corporation is recalling about 4,000 SABRE Aim & Fire Pepper Gel Spray canisters with expiration date 9/2027 because they lack a red nozzle needed to deploy the spray and will not function in an emergency. No injuries have been reported.