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
Keystone is recalling certain 2022 Bullet, Outback, and Passport travel trailers due to improper welds on the coupler hitch. The defect can cause the trailer to separate from the tow vehicle, increasing crash and injury risk.
Volkswagen is recalling certain Atlas and Atlas Cross Sport vehicles because corroded electrical contacts in the front door wiring harness may delay airbag deployment during side impacts, increasing the risk of injury.
Hyundai is recalling 2022 Santa Fe and Santa Cruz vehicles because the turbocharger oil supply pipe may crack, causing an oil leak that could increase fire risk in the engine compartment.
Mercedes-Benz is recalling certain 2021-2022 vehicles with heated leather steering wheels because a software error prevents the DISTRONIC hand-off detection system from functioning. This can disable warnings for drivers to grab the wheel and prevent emergency responder assistance.
Forest River is recalling 2022 Puma and Puma XLE fifth wheel and travel trailer recreational vehicles because the exterior microwave griddle can remain connected to propane when stowed, creating a fire hazard.
Ford is recalling 2022 Lincoln Aviator PHEV vehicles. The inlet charge port harness bus bar may unseat, causing loss of drive power and increasing crash risk.
Ford is recalling 2020-2022 Escape and 2021-2022 Bronco Sport with 1.5L engines. The oil separator housing may crack and leak, creating fire risk near hot engine components.
Ford is recalling 2022 F-150 and related models due to a software error that may disable trailer brake functionality. Loss of trailer brakes increases stopping distance and crash risk.
Boxine US is recalling tonies Blocks wooden toys containing high-powered magnets sold online from November through December 2021. When swallowed, multiple magnets can lodge in the digestive system and cause serious injury or death.
EGL Motor is recalling about 500 EGL and ACE-branded youth ATVs (models MADIX 110 and B125) sold nationwide from May to September 2020 due to violations of federal ATV safety standards. The vehicles exceed speed limits for their age group, have defective brakes, and handlebars that pose laceration hazards in crashes.
Certain 2021-2022 Jeep Grand Cherokee L vehicles may have a missing weld in the child seat tether anchorage system. This could allow the tether to separate during a crash, increasing the risk of child injury.
Commencal Ramones 14-inch children's bicycles lack required foot brakes and are equipped only with hand brakes, posing a crash hazard or risk of injury to young children unable to stop them. About 925 bicycles are affected.
Chrysler is recalling 2021-2022 Pacifica and 2021 Voyager vehicles because the second-row seat mounting latch may fail to secure the seat properly, increasing the risk of injury in a crash.
Sakar International is recalling about 89,000 Dimensions Bluetooth Speaker Helmets sold at Walmart because they do not meet U.S. federal safety standards for bicycle helmets and pose a risk of head injury in a fall.
Segway is recalling about 960 Ninebot children's bicycle helmets because they fail to meet safety standards for positional stability and retention, creating a risk of head injury in a crash. No injuries have been reported.
B. Braun Medical, Inc. is recalling 33,742 bags of 0.9% Sodium Chloride Injection USP due to leaking that compromises sterility assurance. The intravenous medication was distributed nationwide.
Walmart is recalling Avaphinal Maximum Male Enhancement Sexual Pills (2000 MG, 10-capsule cartons, Lot DK1027) distributed nationwide because they contain undeclared sildenafil, making them an unapproved drug.
Family Pharmacy of Statesville is recalling Methylcobalamin 1 mg/mL Injectable in 1 mL syringes (Lot #07282020@3) distributed in North Carolina because the manufacturer cannot assure the product meets sterility standards.
Family Pharmacy of Statesville is recalling Lorazepam 1 mg/mL Infusion Solution in 250 mL bags because the manufacturer cannot assure sterility of the product.
Gourmet Kitchen, Inc. is recalling 43 boxes of Raw Buttermilk Breakfast Tarts due to undeclared almonds. Consumers allergic to almonds should not consume this product.
Family Pharmacy of Statesville is recalling Morphine Sulfate 6 mg/mL infusions in 250 mL bags due to lack of assurance of sterility. The affected product was distributed in North Carolina.
Family Pharmacy of Statesville is recalling four bags of Hydromorphone HCl 1 mg/mL (250 mL each) distributed in North Carolina due to lack of assurance of sterility. The affected lots have beyond-use dates of October 25–30, 2020.
Family Pharmacy of Statesville is recalling one lot of Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags due to lack of assurance of sterility.
Albanese Confectionery is recalling specific lots of its Dark Chocolate Espresso Bean tubs due to undeclared peanut allergen. Consumers with peanut allergies who purchased this product should not consume it.
Family Pharmacy of Statesville is recalling Hydromorphone HCl 2 mg/mL Infusion 250 mL bags (2 units) distributed in North Carolina due to lack of assurance of sterility.