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.
Mercedes-Benz is recalling 2018 S 450 and S560 vehicles because front brake components may have incorrect dimensions, potentially affecting braking performance.
PACCAR is recalling 2020 Kenworth and Peterbilt trucks because improperly heat-treated rear axle output shafts may fracture, creating a road hazard.
BMC is recalling approximately 840 Teammachine SLR01 DISC bicycles and framesets because the fork steerer tube can crack or break, posing a fall hazard.
Subaru is recalling 2016-2017 Outback vehicles because a replacement air bag control module may be incompatible, potentially preventing proper passenger air bag deployment.
Alli & Rose, LLC is recalling approximately 21,930 pounds of Salted Egg Fish Skins because they were imported from Thailand without the required FSIS inspection.
Chrysler is recalling 2020 Jeep Renegade and Fiat 500X vehicles because a fractured right rear brake caliper could fail, reducing braking performance and increasing crash risk.
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because improperly installed lashing rails may detach, potentially allowing cargo to become unsecured and increasing crash risk.
Onset Worldwide is recalling 50 lb bulk bags of Nitro-Milled Black Chia because the product tested positive for Salmonella.
AuroMedics Pharma LLC is recalling Mirtazapine 15 mg tablets that were incorrectly labeled as 7.5 mg. The error affects 500-count bottles distributed nationwide.
Montpak International Inc. is recalling approximately 4,365 pounds of veal and lamb products that were imported into the U.S. without the benefit of import re-inspection.
Cain Food Industries is recalling 2,000 pounds of SLB-R Powder due to possible Salmonella contamination. The product was distributed in seven states.
Cain Food Industries is recalling 2,200 pounds of BETA P-130 due to possible Salmonella contamination. The product was distributed in seven states.
Cook Inc. is recalling 20 CrossCath Support Catheters because a manufacturing error may cause radiopaque marker bands to be too loose or too tight.
Amneal Pharmaceuticals is recalling Ranitidine Tablets 300 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Coast Quality Pharmacy, LLC dba Anazao Health is recalling Clonidine HCL and Morphine Sulfate products due to the presence of Talaromyces rotundus fungi.
Hillsdale Furniture is recalling Chadwick and Bailey five-drawer chests because they can tip over or entrap children if not anchored to the wall.
Harrison Gypsum, LLC is recalling Terra Alba Calcium Sulfate Dihydrate in various bag and bulk sizes due to possible contamination with Salmonella.
Cooper Tire is recalling specific Evolution Tour, Mastercraft, Hercules, Starfire, and Stratus tires due to an improper sidewall component that may cause tire deflation and tread separation.
Forest River is recalling 2020 Georgetown and FR3 motorhomes because improperly tightened trailer hitch bolts may loosen, increasing crash risk.
Amneal Pharmaceuticals is recalling Ranitidine 300 mg tablets because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Anazao Health is recalling compounded fentanyl and morphine drugs after environmental sampling detected Talaromyces rotundus fungi.
Amneal Pharmaceuticals is recalling Ranitidine Syrup Oral Solution because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Coast Quality Pharmacy, LLC dba Anazao Health is recalling Hydromorphone HCL, Baclofen, and Clonidine HCL combination drugs due to fungal contamination found during environmental sampling.
Surgery Pharmacy Services is recalling 1,149 bags of Memorial Central TPN due to a lack of sterility assurance. The product was distributed in Georgia and Tennessee.
Cain Food Industries is recalling ASCORBO 150 Powder due to possible Salmonella contamination. The product was distributed in seven states.