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
Medicina is recalling ENFit 1ml enteral syringes because the plunger was manufactured with polyethylene instead of approved polypropylene. This material defect could affect plunger function and device safety.
Karlsburger Kitchens NSLP 140 Turkey Gravy Mix labeled as gluten-free contains undeclared gluten. The product was distributed in Kansas, Minnesota, Nebraska, and Wisconsin.
Titusville Dairy Products Co. is recalling Turner's Peach Whole Milk Cottage Cheese (5.3oz) distributed in Pennsylvania due to bacterial spoilage. Consumers should not consume the product and should discard it.
Medicina Uk Ltd is recalling Medicina Oral Tip Syringe 2.5ml nationwide because the plunger component was manufactured with polyethylene instead of the approved polypropylene material.
Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Nectar due to indication of product spoilage. Approximately 2094 cases were distributed nationwide.
Porsche is recalling certain 2022 911 GT3 vehicles because the screw attaching the lower seat belt anchor may not have been properly tightened. A loose anchor could detach in a crash, increasing injury risk.
Clorox is recalling Pine-Sol cleaners contaminated with Pseudomonas aeruginosa, a bacteria that risks serious infection in immunocompromised people or those with external medical devices. No illnesses have been reported to date.
CAN-AM is recalling 2019-2023 Ryker motorcycles because electrical harnesses in the front fenders may loosen and rub on the tire, causing a short circuit that can stall the engine while driving.
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.
Winnebago Industries is recalling certain 2020-2023 View and Navion recreational vehicles. The LP fuel line is routed near the rear wheel well and may contact the tire, creating a fuel leak and fire risk.
Tesla is recalling 2017-2022 Model 3 vehicles because second-row seat belt anchors may have been incorrectly reassembled during prior service work. Defective anchors could impair crash protection, increasing injury risk.
The guide bushing on the parking pawl may fatigue and prevent the parking brake from engaging, risking vehicle rollaway. Dealers will provide a free software update to affected 2019-2022 vehicles.
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.
TJX is recalling about 108,000 Mittal International baby blankets sold nationwide from September 2021 through July 2022 because loose threads can detach and pose choking, entrapment, and strangulation hazards to infants.
Gel Blaster is recalling about 62,700 SURGE Model 1.0 toy guns because the lithium-ion battery pack can overheat and ignite. Thirty reports of smoking or fire have been received with no injuries reported.
AQUALUNG is recalling Apeks Exotec SCUBA diving buoyancy compensator devices because the dump valve knob can get stuck when inflated, preventing the device from fully inflating and creating a drowning hazard. Approximately 330 units sold nationwide from August 2021 through June 2022 are affected.
Juvo Plus is recalling butterfly net sets and army action figure playsets because components contain lead and phthalates above federal limits. These chemicals are toxic if ingested by young children and can cause health problems.
Ford is recalling certain 2022 Bronco Sport vehicles due to a fuel pump control module bracket that may not be properly secured to the fuel tank. If the bracket fails, the engine may stall, increasing the risk of a crash.
Backyard Nature Products is recalling Birds Choice acrylic bird baths because sunlight concentrated through the acrylic can overheat nearby wooden surfaces like siding or decking, creating a fire hazard. Two reports of overheating, smoking, fire, and scorching have been received; no injuries reported.
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.
Hobbs Medical is recalling Posi-Stop Injection Needles (lot numbers ending in R) due to incorrect expiration dates on labels that extend shelf life. Affected devices were distributed in the US from March 2018 to September 2020.
Olympus recalls the VC-10 Vacuum Curettage System due to serious injury risk from incompatible collection canisters. The FDA warns users against using accessories not listed in the device's instructions.
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates that extend shelf life, affecting devices distributed in the US and five other countries from 2018 to 2020.