State
73,096 recalls have nationwide distribution and so reach New York. 12,938 additional recalls listed New York specifically in their distribution scope.
Of the 12,938 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,148 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,938 recalls whose distribution notice names New York specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling certain 2018-2021 GL1800 Goldwing motorcycles because the primary drive gear bolt on the crankshaft may break, causing an engine stall and locking the rear wheel.
International is recalling certain 2021-2025 trucks with Bendix EC80 control units because electrical noise may cause the ECU to misprocess commands or stop working, disabling ABS and stability control.
Altec Industries is recalling 2022-2024 AC series cranes because improperly manufactured outrigger shoes may crack and fail, reducing stability and increasing injury risk.
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.
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.
GM is recalling certain 2020-2022 Bolt EV and 2022 Bolt EUV vehicles previously repaired under 21V-650, because diagnostic software installation may have failed, so the battery could catch fire at high charge.
Mazda is recalling certain 2024-2025 CX-90 and 2025 CX-70 vehicles with a Dash Electrical Supply Unit because the defroster, seat belt warning, 360° view monitor and PHEV battery cooling may not work at startup.
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.
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.
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.
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.
Volkswagen is recalling specific Beetle and Passat models because the driver's side air bag inflator may explode, posing a risk of serious injury or death.
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.
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.
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 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'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.
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.
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.
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.
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.
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.
Medtronic Neuromodulation is recalling the SynchroMed II Infusion Pump (Product Number 8637-20) due to potential data corruption in the pump's memory that could prevent proper interrogation of the device.
Medline is recalling certain medical procedure kits packaged in breather pouch lot 323080002 because seals may not prevent non-sterile product use. Affected units were distributed in the US, Canada, and Panama.
Datex-Ohmeda Amingo anesthesia systems may allow a patient breathing circuit to be mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) instead of the proper outlet. The potential misconnection affects all 77 units worldwide.