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.
Entropic Labs is recalling SARM RAD-140 capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Palodex Group Oy is recalling Instrumentarium Dental Express X-ray imagers because slow degradation of plastic insulation in the power supply unit may cause short circuits, heating, and smoke.
Mercedes-Benz is recalling certain 2018-2019 AMG vehicles because a turbocharger oil feed line may leak, increasing the risk of a fire.
Chrysler is recalling 2020 Jeep Wranglers because a front suspension weld may be improperly positioned, increasing the risk of a crash.
Chrysler is recalling 2019-2020 Ram 2500 and 3500 pickups because transmission fluid leaks may contact ignition sources, increasing the risk of a fire.
Golden Pearl Trading Corporation is recalling approximately 12,054 pounds of ready-to-eat imported salted egg fish skin products that were not presented for import re-inspection.
Rosenbauer America is recalling 2014-2019 Commander vehicles because front shocks may separate, potentially damaging the steering gear and causing a loss of power steering assist.
General Motors is recalling 2014-2015 Cadillac CTS-V Sport vehicles because rear-axle differential roll pins may fracture, potentially causing the driver to lose control.
Mitsubishi is recalling 1998-2000 Montero vehicles because air bag inflators may rupture or underinflate in a crash, increasing injury risk.
Chrysler is recalling 2014-2019 Ram ProMaster vans because the transmission shifter cable may disconnect, causing unintended vehicle movement and crash risk.
Keystone RV is recalling 2020 Crossroads trailers because improper WiFi wiring circuit protection may increase the risk of fire during a short circuit.
Assurance Infusion is recalling LIPO B 25MG/50MG/50MG/1000MCG/ML products due to a lack of sterility assurance. The recall covers nationwide distribution.
Toyota is recalling 1997-2000 Celica, RAV4, and Supra vehicles because driver air bag inflators may rupture or underinflate in a crash.
Assurance Infusion is recalling Fentanyl and Sufentanil Injection in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling a specific lot of buprenorphine and fentanyl injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling Morphine Sulfate Injection in 20 mL syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of a multi-drug injection syringe due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Morphine 5mg/mL injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling specific syringes of a multi-drug injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Buprenorphine and Fentanyl injection due to a lack of sterility assurance.
Assurance Infusion is recalling Fentanyl 3000mcg/mL injection syringes due to a lack of sterility assurance. The affected lots were distributed nationwide.
Assurance Infusion is recalling 45 vials of Trimix Super injection nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling 19 vials of CJC-1295 and Ipamorelin injections nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling Fentanyl 100mcg/mL injection syringes nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Baclofen and Hydromorphone injection due to a lack of sterility assurance. The affected product was distributed nationwide.