Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. 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.
Wells Pharmacy Network LLC is recalling 22 vials of a compounded injectable drug due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 35 vials of TriMix compounded injections because the agency cannot assure the products are sterile.
Hale And Hearty Soups, LLC is recalling White Bean, Broccoli S.D.T. soup due to potential contamination with Listeria monocytogenes.
Subaru is recalling 2005-2008 models and 2006 Saab 9-2X vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Mercedes-Benz is recalling specific 2008-2012 models because front passenger air bag inflators may rupture during deployment, potentially sending metal fragments into the vehicle.
Tesla is recalling 2012 Model S vehicles because the front passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.
Jaguar Land Rover is recalling 2007-2012 Range Rovers because front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Subaru is recalling specific 2005-2012 models because front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Mitsubishi is recalling 2012 and 2014 i-MiEV vehicles because front passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.
Honda is recalling specific 2006-2012 models because the front passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Perfect Fit Meals is recalling approximately 3,546 pounds of chicken breast product because it contains undeclared milk and wheat allergens.
Mazda is recalling 2007-2009 B-Series trucks because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.
Ford is recalling specific 2005-2012 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Jaguar is recalling specific 2009 and 2012 XF vehicles because the passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.
Nissan is recalling specific Infiniti and Nissan Versa vehicles because the front passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
McLaren is recalling 2012 MP4-12C Spider vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Schreiber Processing Corp. is recalling approximately 2,330 pounds of chicken tenders that may contain plastic and are misbranded. The products were distributed in New Jersey, New York, and Washington.
Toyota is recalling specific 2006-2012 models because passenger air bag inflators may rupture in a crash, potentially sending metal fragments into the cabin.
Karma Automotive is recalling 2012 Fisker Karma vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Sunset Natural Products Inc. is recalling Nutra Pro dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Abte bulk capsules pursuant to a consent decree requiring the destruction of dietary supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Extra Mega Prostamax dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Nutriplex Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Collagen 300 mg capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Foni bulk capsules pursuant to a consent decree requiring the destruction of dietary supplements manufactured since April 2014.