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
Thor Motor Coach is recalling 1,969 Palazzo recreational vehicles from model years 2015–2023 because front brackets supporting the fiberglass panel may become loose and detach while driving, creating a road hazard.
Certain 2022-2023 Isuzu, Chevrolet, and Hino commercial vehicles with improperly calibrated ABS and optional ADAS camera systems are being recalled. The miscalibration could prevent the automatic emergency braking and electronic steering control systems from functioning properly, increasing crash risk.
Ford is recalling certain 2023 Bronco Sport vehicles because valves inside the ABS module may have been damaged during manufacturing, causing an internal leak. This can lead to unexpected brake pedal travel or unexpected movement, increasing crash risk.
Altec is recalling certain 2004-2023 AT Series aerial devices because cables in the engine compartment may contact the hood, damaging the cables and causing a short circuit that increases fire risk. Free repair available through Altec.
Ford is recalling 2021 Lincoln Aviators with 360-degree camera systems because the rearview camera video may fail to display, reducing driver rear visibility and increasing crash risk.
Autocar is recalling certain 2020-2023 Xpeditor vehicles because the external sun visor may obstruct roof-mounted clearance lights. The obstruction may increase crash risk.
Autocar is recalling 2021-2023 Xpeditor natural gas vehicles due to a software error in the instrument cluster fuel gauge. The inaccurate fuel gauge may cause the vehicle to unexpectedly run out of fuel and stall, increasing crash risk.
Subaru is recalling 2022 WRX vehicles with Eyesight because the owner's manual contains incorrect instructions for adjusting the High Beam Assist function. Owners will receive a corrected manual insert by mail.
Sanven Technology is recalling about 420 Vevor Baby Gates sold online from February to May 2024. The gates violate federal safety regulations because a child's torso can fit through the opening between the gate slat and side wall, creating an entrapment hazard.
Polaris is recalling about 1,400 Model Year 2023-2024 Ranger XP Kinetic recreational off-road vehicles because loose high voltage cables on the motor controller unit can arc or overheat, posing fire and crash hazards.
Manhattan Comfort is recalling about 46,750 floating wall theater entertainment centers because panels can detach and fall when not properly installed with toggle bolts or safety screws. The firm has received 51 reports of panels detaching, including three minor injuries.
HALO Branded Solutions is recalling about 60,000 reusable tumblers with metal straws sold at Wawa stores due to a laceration hazard. The metal straw can cut the mouth and fingers; four injuries have been reported.
Harbor Freight Tools recalls about 53,000 Bauer 20V Battery-Powered 4-Gallon Backpack Sprayers because the pump can leak chemicals into the battery compartment, causing the battery to overheat and catch fire. Eight reports of battery overheating, smoking, melting, and fire have been received; no injuries reported.
Humane Inc. is recalling about 10,500 Charge Case Accessory units for the Ai Pin because the lithium battery can overheat and pose a fire hazard. The company has received one report of a charge case overheating and melting during charging, though no injuries or property damage have been reported.
Datex-Ohmeda Aisys anesthesia machines may allow patient breathing circuits to be incorrectly connected to the Auxiliary Common Gas Outlet, potentially affecting ventilation during anesthesia. Approximately 4,790 units worldwide are affected.
Datex-Ohmeda Aespire 100 anesthesia machines are recalled due to potential misconnection of breathing circuit limbs to the Auxiliary Common Gas Outlet port, which could impair anesthesia or ventilation delivery.
Datex-Ohmeda's Aisys CS2 anesthesia machine may pose a risk if a patient breathing circuit limb is mistakenly connected to the Auxiliary Common Gas Outlet port. Ninety-two units worldwide are affected in this FDA Class I recall.
Datex-Ohmeda has recalled 12,036 Aespire 7900 anesthesia gas machines worldwide due to potential risk of patient breathing circuit being mistakenly connected to the Auxiliary Common Gas Outlet port.
Avance CS2 and Avance CS2 Pro anesthesia machines may permit breathing circuit misconnection to the wrong gas outlet. Affected devices have the AGCO option and are distributed worldwide.
Datex-Ohmeda is recalling approximately 15,739 Aisys CS2 anesthesia machines worldwide. A breathing circuit limb may be mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port instead of the intended connection point.
Choi's Kimchi LLC recalled Gluten Free Gochujang Red Chili Paste due to Salmonella. The recall affects 11 cases distributed in Oregon and Washington.
Datex-Ohmeda is recalling 20,097 Aespire 7100 series anesthesia machines because a patient breathing circuit can be mistakenly connected to the wrong outlet (ACGO port) instead of the intended connection point.
Datex-Ohmeda is recalling Avance anesthesia gas machines worldwide due to a potential hazard if a patient's breathing circuit is incorrectly connected to the Auxiliary Common Gas Outlet port during setup.
HP Hood LLC is recalling Lactaid Lactose Reduced milk products because they may contain undeclared almond from almond milk. People with almond allergies face serious health risks.
Baxter Healthcare recalls Life2000 Ventilators due to potential Low Gas Pressure alarm failure. The alarm may not activate if the gas source isn't connected before therapy begins.