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.
Sunset Natural Products Inc. is recalling Nixin Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Western United Fish Company is recalling Limu Poke kits due to potential Salmonella contamination from affected seaweed.
Sunset Natural Products Inc. is recalling Strev bulk capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Test Booster dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Neurocetin Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2014.
Sunset Natural Products Inc. is recalling Marx Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Liver Clean Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Growlean Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2014.
Sunset Natural Products Inc. is recalling Madre Cell dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling 1,530,000 units of Gludo bulk capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Nees bulk capsules pursuant to a consent decree requiring the destruction of dietary supplements manufactured since April 2014.
Volkswagen Group of America is recalling specific Audi models because a blocked coolant pump can overheat and cause a fire.
REV is recalling 2017 Fleetwood and Holiday Rambler motor homes because the rear sway bar may detach, increasing crash risk.
Volkswagen Group of America is recalling 2011-2017 Audi Q5 vehicles because water in the sunroof drainage system may corrode side air bag inflators, posing a risk of serious injury.
Ford is recalling 2017 F-250 and F-350 Super Duty trucks because a missing frame reinforcement bracket may allow the fuel tank strap to separate, increasing fire risk.
Glacier is recalling 38 model year 2016 RV Explorer trailers because a short axle bolt may fail, causing the wheel assembly to detach and increasing crash risk.
Jaguar Land Rover is recalling 2016-2017 Range Rover, Range Rover Sport, and 2017 Discovery Sport vehicles because front seatbelt pretensioners may not function properly in a crash.
Jaguar is recalling 2016-2017 XJ vehicles because the front passenger air bag may fail to deploy in a crash. Dealers will replace the air bag free of charge.
Volkswagen Group of America is recalling specific 2016-2018 Audi and Volkswagen models because air bags or seat belt pretensioners may not function properly in a crash.
Woodland Foods is recalling salt-free roasted sunflower seeds potentially contaminated with Listeria. The product was distributed to food distributors in 25 states.
Wakefern Food Corp. is recalling 24-pack Gourmet Red Velvet Cookies because they may contain metal pieces. The product was distributed in six states.
Impax Laboratories is recalling 3,074 boxes of Lamotrigine Orally Disintegrating Tablets because some 200 mg boxes contained 100 mg tablets.
Midwest International Corp is recalling 80 cartons of canned fish because the product lacks a registered manufacturer and scheduled process.
Virtus Pharmaceuticals is recalling 24,444 bottles of Hyoscyamine Sulfate tablets because they failed content uniformity specifications, resulting in inconsistent drug potency.
Oscor, Inc. is recalling 255 Breezeway sheaths because a fragment of the inner liner detached during insertion, posing a risk of injury.