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.
Daimler Trucks North America is recalling 2015-2017 Freightliner models because a missing check valve could cause sudden parking brake application and increase crash risk.
Overhill Farms is recalling approximately 54,630 pounds of frozen chicken bites products due to possible contamination with bone fragments.
Honda is recalling 2018 Odyssey vehicles because the third-row center seat belt tongue may not latch securely, increasing injury risk in a crash.
Continental Automotive Systems is recalling fuel pump flanges for Volkswagen, Audi, and Porsche vehicles because they may crack and leak fuel, increasing fire risk.
Gilster-Mary Lee Corp. is recalling Western Family Onion Soup Mix because it may contain undeclared egg. The product was distributed to Associated Foods Stores in Utah.
Bright Farms is recalling 4oz packages of Baby Romaine salad due to detected metal contamination. The firm identified the issue through internal verification.
Aston Martin is recalling 2012 V8 Vantage vehicles because a transmission connector may break, causing a fluid leak that could prevent shifting or cause the vehicle to roll away.
The Horton Fruit Co is recalling specific bags and totes of spinach sold as Harris Teeter and Peak brands due to possible listeria contamination.
Creganna Medical Devices is recalling 50 units of Boston Scientific Zurpaz Steerable Sheaths due to a lack of sterility assurance.
Medtronic is recalling custom suture packs because an incomplete inner package seal may cause the suture material to degrade prematurely.
Creganna Medical Devices is recalling 85 units of Boston Scientific Zurpaz Steerable Sheaths due to a lack of sterility assurance.
Safecor Health LLC is recalling 856 bottles of Doxycycline 100mg tablets in Massachusetts and New York due to Current Good Manufacturing Practice (CGMP) deviations.
Aston Martin is recalling 2011-2014 V8 Vantage vehicles because a broken clutch fluid line connector may cause hydraulic leaks, preventing gear shifting or causing the vehicle to roll away.
Bausch & Lomb is recalling specific lots of NasalCrom nasal spray due to potential microbial contamination in the manufacturing water.
GE Healthcare is recalling Infant Warmer Systems because loose screws in the heater head could fall and cause thermal injuries to patients.
Cummins is recalling X15 heavy-duty diesel engines because a fuel pump drive gear may slip, causing engine stalls and increasing crash risk.
Embutidos Fanguito, Inc. is recalling pork products due to mislabeling, misbranding, and undeclared allergens. The products were distributed to retail locations in Florida.
KTM is recalling 2016-2017 690 Duke motorcycles because the fuel tank filler cap area may leak, increasing the risk of fire or injury.
Entegra is recalling 2012-2015 Cornerstone motorhomes because a starter motor component may break, causing overheating and increasing the risk of a fire.
Triple E RV is recalling 2016-2017 Wonder motorhomes because missing frame bolts may cause structural distortion and affect vehicle control.
Embutidos Fanguito, Inc. is recalling approximately 454 pounds of sliced pork ham products due to mislabeling, misbranding, and undeclared allergens.
Thor Motor Coach is recalling 2018 Outlaw 29H motorhomes because an incorrect fuse size may increase the risk of a fire if the awning light circuit short circuits.
Arrow International is recalling VPS Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets because connection issues may cause leaks and contamination, potentially leading to peritonitis.
Arrow International is recalling MAC Two-Lumen Central Venous Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.