Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Reser's Fine Foods is recalling Caesar Salad Kits due to Listeria monocytogenes contamination in the cooked chicken component. The recall affects 21,098 cases distributed across 31 U.S. states.
Lucid is recalling 2024-2025 Air models due to a rear subframe wiring harness that may be too short, causing power loss to the rear drive unit and increasing crash risk. Replacement is free.
Polestar is recalling 2020 Polestar 1 vehicles because the brake pedal may detach from the brake booster, increasing crash risk.
Tesla is recalling 2024 Cybertruck vehicles due to a drive inverter fault that may cause loss of propulsion. Affected owners will receive a free inverter replacement.
Kawasaki is recalling 2024 Ninja 7 Hybrid and Z7 Hybrid ABS motorcycles because a frame weld may crack, causing loss of control.
International is recalling 2024-2025 HX vehicles because insufficient lubricant in front axle hubs may damage wheel bearings, potentially causing wheel separation and loss of control.
Continental Automotive is recalling MK C1 EVO brake systems where a fastener may be improperly assembled, causing the brake pedal to detach and increasing crash risk.
KZRV is recalling 2025 Sportsmen 303QBSE travel trailers because the driver's side slide-out actuator is too close to the tires, posing a crash risk.
Forest River is recalling 2025 East to West Alta travel trailers because an incorrectly wired inverter may increase the risk of fire.
Mazda is recalling certain 2024 CX-90 and 2025 CX-70 vehicles because powertrain and engine control module software may illuminate malfunction lights and cause a loss of drive power.
Mazda is recalling certain 2024 CX-90 and 2025 CX-70 plug-in hybrids because improper inverter software may illuminate malfunction lights and cause a loss of drive power in EV mode.
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.
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.
Mazda is recalling 2024 CX-90 vehicles because a software issue may prevent the engine from restarting after the i-stop feature turns it off, increasing crash risk.
Outdoors RV is recalling 340 2025 travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing the risk of injury or fire.
Baxter Healthcare is recalling 13 TruSystem 7000 operating tables because their batteries and connectors experienced electrical short-circuits and emitted smoke.
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.
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.
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.
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.
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 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.