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 Aloe Vera 500 mg bulk capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Aloe & L Glutamine Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Publix is recalling Blueberry Flavored Pancake & Waffle Mix because the milk powder ingredient may contain Salmonella.
Sunset Natural Products Inc. is recalling Crea Care capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Bioxtron Dietary Supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Sunset Natural Products Inc. is recalling Natural Fat Burner capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Via Sex Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Magnumn dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Artrosamin capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.
Sunset Natural Products Inc. is recalling Ramto bulk capsules pursuant to a consent decree requiring the destruction of dietary supplements manufactured since April 2014.
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.