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.
Highland Ridge RV is recalling 2015-2016 travel and fifth wheel trailers because incorrect Gross Vehicle Weight Rating labels may allow overloading, increasing the risk of tire failure and crashes.
Daystar is recalling aftermarket rear control arm brackets for 2015-2016 Jeep Renegades due to improper welds that may allow the rear axle to shift, increasing crash risk.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, posing a risk to consumers with milk allergies.
E3 Artisan is recalling 40 bars of 3-piece Blood Orange Meltaways because FDA samples tested positive for undeclared milk.
Volvo is recalling 2016-2017 VNL, VNX, and VNM trucks because a missing roll pin or loose bolt may cause the steering shaft to separate, resulting in a loss of steering.
E3 Artisan is recalling Meltaway bars because FDA testing found undeclared milk, a major allergen, in the product.
E3 Artisan is recalling specific dark chocolate bars because FDA samples tested positive for undeclared milk, a major allergen.
Goodman Company is expanding a recall for specific air conditioning and heating units because their power cords can overheat, posing fire and burn risks.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, a major food allergen.
E3 Artisan is recalling Mendiant dark chocolate bars because FDA testing found undeclared milk, a major allergen, in the product.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, a major food allergen.
Mevion Medical Systems is recalling four MEVION S250 Radiation Therapy Systems because the treatment table positioning belt can slip, causing patient setup deviations.
E3 Artisan is recalling dark chocolate bars because FDA testing found undeclared milk, a major allergen, in the product.
E3 Artisan is recalling 30-bar packages of Tahitian Vanilla Lemon Meltaways because FDA testing found undeclared milk on the labels.
E3 Artisan is recalling dark chocolate bars containing candied ginger, orange peel, and coriander because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Meltaway bars because FDA samples tested positive for undeclared milk, a major food allergen.
Philips is recalling two Allura Xper FD OR Tables because the C-arc may continue moving after stopping due to improper adjustment.
Pharmedium Services, LLC is recalling 19 syringes of Morphine Sulfate in Wisconsin because the drug was found to be subpotent.
C.R. Bard is recalling Arctic Sun 5000 and 2000 devices because a simulator key could be connected to the patient cable, resulting in improper temperature therapy.
E3 Artisan is recalling 3-piece peppermint meltaways because FDA samples tested positive for undeclared milk.
Smith & Nephew is recalling BEAVER Blade 4.0mm orthopedic instruments because they may fracture during hip arthroscopy procedures.
FreshPoint Corporate is recalling sliced cucumbers in Florida and Georgia due to possible Salmonella contamination.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk on the labels.
E3 Artisan is recalling 636 dark chocolate bars because FDA testing found undeclared milk, a major food allergen, in the product.
E3 Artisan is recalling Mendiant Orange apricot and caramelized hazelnut chocolate bars because FDA samples tested positive for undeclared milk.