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.
WP Dynamics is recalling ReadyLIFT Lift Kits for certain Ford and Dodge trucks because improperly heat-treated bolts may break, risking suspension separation and loss of vehicle control.
Volkswagen is recalling 2018-2019 Atlas vehicles equipped with specific Continental tires that may have been over-cured during production, posing a risk of sudden air loss or loss of vehicle control.
Ford is recalling 2021 Mustang Mach-E vehicles because front subframe bolts may not have been tightened properly, which could reduce crash performance and increase injury risk.
Mitsubishi is recalling 2013-2015 Outlander Sport vehicles in 23 states because the front cross member may corrode, causing the front lower control arms to detach.
Ferrara Fire Apparatus is recalling 2019-2020 Inferno vehicles because steering gear mounting bolts may loosen, causing steering difficulties and increased crash risk.
Nissan is recalling certain 2020-2021 Altima vehicles because the tie rod ball joint fastener was not tightened properly. This could cause the fastener to detach and result in loss of steering control.
Certain 2017-2021 Sportage and 2017-2019 Cadenza vehicles have a defective hydraulic control unit that may short-circuit and ignite an engine compartment fire. Owners should park outside until repairs are completed.
Teva Pharmaceuticals is recalling specific lots of Vecuronium Bromide for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Dacarbazine for Injection USP because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Hong Thai Foods Corp is recalling Golden Boy Custard Muffin Banana packages due to undeclared milk discovered during New York state sampling.
Teva Pharmaceuticals is recalling 6,710 vials of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Toposar (etoposide) injection vials because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling specific lots of Sterile Diluent for Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
CareFusion 213, LLC is recalling ChloraPrep One-Step antiseptic applicators distributed in Puerto Rico and Oman due to potential fungal growth and package integrity breaches in hot, humid climates.
CareFusion 213, LLC is recalling Chloraprep One-Step applicators distributed in Puerto Rico and Oman due to potential fungal growth in hot, humid conditions.
Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
DeRoyal Industries is recalling 309 CV Basin Set Packs because the included sternum saw blades are not sterile.
Steris is recalling 272 OT1000 Series Orthopedic Surgical Tables because a glued bond may separate, potentially causing unexpected movement during procedures.
Barbara's Orchard/Delicae Gourmet is recalling Thai Peanut Sauce due to undeclared shrimp. Consumers should stop using the product and return it to the store.
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Metoclopramide Injection because manufacturing areas exceeded microbial acceptance levels, creating a lack of sterility assurance.
Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Desmopressin Acetate Injection because manufacturing areas exceeded microbial limits, compromising sterility assurance.
Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Porsche is recalling certain 2015-2018 Macan models because the front passenger seat occupancy sensor may fail to detect a passenger, preventing the air bag from deploying.