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.
Volvo is recalling 2011-2017 S60 and V60 models because a door latch component may break, potentially allowing doors to open while driving.
BMW is recalling 1999-2000 323i, 328i, 323Ci, and 328Ci vehicles because driver air bag inflators may rupture or underinflate in a crash, increasing injury risk.
BMW is recalling 1999-2001 3-Series vehicles because a replacement driver air bag inflator may absorb moisture, potentially causing it to rupture or underinflate during a crash.
Forest River is recalling 2018-2020 Cascade and Cherokee travel trailers because the trailer hitch coupler may fail, potentially causing the trailer to detach from the tow vehicle.
Jayco is recalling 2018-2020 Melbourne Prestige motorhomes because defective propane tank hangers may allow the tank to dislodge, increasing crash and fire risk.
The Toro Company is recalling 2017-2019 LC922 towable log splitters because tow bolts may fail, causing the unit to detach or tip over.
Entegra is recalling 2018-2020 Qwest motorhomes because defective propane tank hangers may allow the tank to dislodge, increasing crash and fire risk.
Transportation Collaborative is recalling 2019-2020 TransTech school buses because the roof hatch handle may break, preventing emergency exit.
General Motors is recalling 2020 Cadillac, Chevrolet, and GMC vehicles because a missing fuel pump pressure regulator may cause over-pressurization and fire risk.
Navistar is recalling 2020 International HV 6X4 vehicles because a non-Quick Release Modulator Valve may increase brake release time, raising the risk of brake or tire fires.
Morris Meat Packing is recalling approximately 515,000 pounds of raw pork products produced without federal inspection. The products were distributed in Illinois.
Viatrexx Bio Incorporated is recalling Viatrexx-Adipose vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide.
California New Foods is recalling 8,923 cases of Carolyn's Cookie Company Frozen Oatmeal Raisin Cookie Doughballs due to a consumer complaint of an allergic reaction.
Viatrexx Bio Incorporated is recalling 19 vials of Viatrexx-Ouch because the manufacturing process cannot guarantee sterility.
Viatrexx Bio Incorporated is recalling Viatrexx-Lymph 1 vials because the manufacturing process cannot guarantee sterility.
Apotex Inc. is recalling Equate Maximum Strength Ranitidine Tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA). The recall covers 1,132,453 bottles distributed nationwide.
Viatrexx Bio Incorporated is recalling Viatrexx-Infla vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide and in Puerto Rico.
Viatrexx Bio Incorporated is recalling Viatrexx-Neuro 3 vials because the manufacturing process cannot guarantee sterility.
Viatrexx Bio Incorporated is recalling Viatrexx-Articula vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide and in Puerto Rico.
Novitium Pharma LLC is recalling Ranitidine Capsules 300 mg because of the presence of the NDMA impurity. The recall covers 6,660 bottles distributed nationwide.
Viatrexx Bio Incorporated is recalling Viatrexx-Systemic Detox vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide.
Novitium Pharma LLC is recalling 2,718 bottles of Ranitidine Capsules 150 mg because the product contains the NDMA impurity.
Isuzu is recalling certain 2017-2020 Isuzu and Chevrolet trucks because rear outer wheel lug nuts may not have been properly tightened, increasing crash risk.
California New Foods is recalling 8,923 cases of Carolyn's Cookie Company Frozen Cookie Doughballs due to a consumer complaint of an allergic reaction.
Apotex Inc. is recalling Walgreens Regular Strength Wal-Zan 75 tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA).