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.
Ring is recalling approximately 350,000 2nd Generation Video Doorbells because incorrect installation screws can cause the battery to overheat, posing fire and burn risks.
Sunjoy is recalling Oakmont LP fire pit tables sold at Big Lots because an incorrectly installed hose can melt and ignite, posing a fire hazard.
Forest River is recalling 2019-2020 Rockport work trucks because the battery box may be inadequately welded and detach, increasing crash risk.
Autocar is recalling 2020-2021 Xpeditor and Legend vehicles because transverse torque rod mounting bolts may not be properly tightened. If bolts fail and disconnect, vehicles could lose suspension control, increasing crash risk.
Daimler Trucks North America is recalling 2019-2021 Freightliner Econic SD vehicles because damaged electrical cables may cause a fire or engine stall.
Jaguar Land Rover is recalling 2020 Discovery Sport and Range Rover Evoque MHEV vehicles because an electrical short-circuit could cause a fire.
Bausch Health is recalling 35,424 tubes of Hydrocortisone butyrate Cream, 0.1%, because the product was found to be subpotent.
RemedyRepack Inc. is recalling Metformin Hydrochloride Extended Release 750 mg tablets because of detected NDMA impurity levels above acceptable intake limits.
W L Gore is recalling GORE TAG CONFORMABLE Thoracic Stent Grafts because a secondary deployment fiber attachment prevented completion of deployment via the access hatch.
Alliance Outdoor Products is recalling about 3,400 climbing treestands because cable assemblies can separate due to corrosion, posing a fall hazard.
Certain 2020-2021 BMW X5, X6, X7, and related models have a front axle support weld that may separate, potentially affecting vehicle handling and control and increasing crash risk.
Toyota is recalling over 1.5 million vehicles because a fuel pump defect may cause the engine to stall while driving, increasing crash risk.
Volvo is recalling 2001-2003 S60 and S80 vehicles because the driver-side air bag inflator may rupture, sending metal fragments into the vehicle.
Triple E RV is recalling 143 Wonder motorhomes because a control center component can overheat and cause a fire.
Kawasaki is recalling 2018-2020 Ninja H2 SX motorcycles because a software defect may cause gear fracture and engine lockup, increasing crash risk.
Mercedes-Benz is recalling 2019 GLA 250 vehicles because a loose engine compartment fusebox may damage fuses and disrupt critical safety systems, increasing crash risk.
Triple E RV is recalling 2019-2021 motorhomes because an incorrect brass connector on the water heater may cause a propane leak, increasing fire risk.
Jayco is recalling certain 2020-2021 Northpoint recreational trailers due to potential axle spindle weld failures that could cause wheel separation and increase crash risk.
General Motors is recalling specific 2018-2020 vehicles because missing bolts on the start/stop accumulator may cause transmission leaks, loss of propulsion, or fire.
BMW is recalling 2020-2021 M2 and 2020 M4 Coupes because missing fuel injector components may cause vibration, leading to fuel leaks and fire risk.
Mueller Austria is recalling Onion Chopper Pro units because a locking tab can detach, allowing hands to slide into the blades. The company reported 137 laceration injuries.
Stryker Neurovascular is recalling Trevo XP ProVue Retriever devices due to increased fracture complaints of the core wire, which can cause the stent retriever to separate and remain in the patient's vasculature.
Sauer Brands Inc is recalling The Spice Hunter Cilantro jars due to potential Salmonella contamination. The product was distributed nationwide and online.
High Quality Organics is recalling organic parsley after a customer test confirmed the presence of Salmonella.
Baxter Healthcare is recalling 152,539 SIGMA Spectrum Infusion Pumps to update the Instructions for Use (IFU) regarding cleaning practices.