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.
Coastal Meds, LLC. is recalling 1,457 vials of LIPO-DEN PLUS Injectable because of the presence of unknown particulate matter. The product was distributed nationwide in the USA.
Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.
Chrysler is recalling 2018 Jeep Cherokee vehicles with 2.4L engines because a fuel tube may leak, increasing the risk of a fire.
Chrysler is recalling 2018 Jeep Compass vehicles because front lower control arms may be incorrectly welded, potentially causing separation and loss of vehicle control.
Chrysler is recalling 2004-2007 Jeep Liberty vehicles because rear suspension lower control arms can fracture due to corrosion, potentially causing a loss of vehicle control.
Chrysler is recalling specific Mopar Gooseneck Ball Kits because the retention ball may detach from the truck, increasing the risk of a crash.
Chrysler is recalling 2018 RAM 4500 and 5500 trucks because brake hose ferrules may lack anti-corrosion plating, potentially causing fluid leaks and loss of braking.
Chrysler is recalling 2018 Dodge, Jeep, Chrysler, and RAM vehicles because an incorrect transmission park lock rod may prevent the vehicle from staying in Park, increasing crash risk.
Chrysler is recalling 2015-2018 Dodge Charger pursuit police vehicles because the front driveshaft may detach, creating a road hazard and increasing crash risk.
Ford is recalling 25,658 2015-2017 Transit vehicles with trailer tow modules because water intrusion can corrode wiring, potentially causing electrical shorts, fires, or crashes.
Mercedes-Benz is recalling specific 2012-2017 SUVs because oil in the Active Curve System may leak and cause a fire if the level is low.
Mercedes-Benz is recalling 2008-2009 Smart Fortwo vehicles because a rear insulation mat may contact hot exhaust components, increasing fire risk.
Forest River is recalling 2018 Starcraft Bus XLT and Glaval Bus Concorde II models because a gear shift cable clip may not be properly seated, potentially causing the vehicle to roll or shift unexpectedly.
Advance Stores is recalling ToolWorks TW1489 Fuse Kits sold at Advance Auto Parts and Carquest because the fuses may fail to protect circuits, increasing fire risk.
ZF North America is recalling certain axles with radial air disk brakes because a broken guide pin support bolt may cause loss of braking ability or tire pressure.
Honda is recalling 2017 Civic Hatchback and Type R vehicles because replacement seatback pads may block side air bags, increasing injury risk in a crash.
Partell Specialty Pharmacy is recalling Estradiol 55 mg pellets in Nevada due to a non-approved sterilization method.
Autochair is recalling Milford Smartbase units because a weak spring and misaligned locking pin caused legs to fold, dropping a person.
Partell Specialty Pharmacy is recalling Lipoic Acid 25mg/mL vials in Nevada because the firm used a non-approved method of sterilization.
Partell Specialty Pharmacy is recalling Estradiol 50 mg pellets in Nevada due to a non-approved sterilization method.
Blue Bird is recalling 2018-2019 All American and Vision transit buses because air brake gauges may incorrectly display 0 PSI, increasing crash risk.
Philips is recalling 19 Brilliance iCT SP CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.
Partell Specialty Pharmacy is recalling Estradiol 35 mg pellets in Nevada due to the use of a non-approved sterilization method.
Partell Specialty Pharmacy is recalling specific lots of Testosterone/Anastrozole pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling TM #6 drug products in Nevada due to a non-approved method of sterilization.