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 Vans USA is recalling 2015-2017 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because driver air bag inflators may explode during deployment.
Motor Coach Industries is recalling specific 1997-2015 coaches because a steering defect may cause loss of control at highway speeds.
Keystone RV is recalling 2017-2019 Dutchmen Voltage and 2019 Endurance travel trailers because tires may contact the rear floor support, affecting handling.
Ford is recalling specific 2010-2014 models because passenger air bag inflators may explode due to humidity, posing a serious injury risk.
Tesla is recalling 2014-2016 Model S vehicles because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Vantage Mobility International is recalling 2014-2017 AMS Edge II vehicles because a deteriorating fuel pump gasket may cause fuel leaks, increasing fire risk.
Ford is recalling 2019 EcoSport vehicles because improperly welded front seat frames may cause the seat back to be loose, increasing injury risk in a crash.
Arcimoto is recalling 2018 FUV motorcycles because incorrect machining of the transmission case may cause premature gearbox failure, potentially immobilizing the vehicle and increasing crash risk.
Arcimoto is recalling 2017-2018 FUV motorcycles because the front suspension and steering system may loosen or wear, potentially causing a loss of steering control.
Arcimoto is recalling 2017 FUV motorcycles because the brake system design may fail to meet federal stopping distance requirements, increasing crash risk.
R. L. Zeigler Co. is recalling Red Hot chicken and pork sausage products due to possible metal contamination. No illnesses have been reported.
Hyundai is recalling 2011-2014 Sonata and 2013-2014 Santa Fe Sport vehicles because a fuel pipe may leak, increasing the risk of a fire.
Luckyberry is recalling unpasteurized Spicy Ginger cold-pressed juice sold in Lawrence, KS, due to a violation of FDA juice safety regulations.
Luckyberry is recalling unpasteurized cold-pressed juice sold in Lawrence, Kansas, due to violations of FDA juice safety regulations.
COVIDIEN LLC is recalling 9,593 Puritan Bennett 980 ventilators worldwide due to a software update affecting external USB drive performance and GUI functionality.
Luckyberry is recalling cold-pressed juice products sold in Lawrence, KS, because they were manufactured and distributed in violation of FDA regulations requiring pasteurization.
Enovachem is recalling Dyural-80 Injection Kits because the product insert incorrectly stated that the stoppers do not contain latex, when they actually contain natural rubber latex.
Tris Pharma is recalling specific lots of Infants' Ibuprofen because they may contain a higher concentration of the active ingredient.
Luckyberry is recalling unpasteurized cold-pressed juice products distributed in Lawrence, Kansas, due to violations of FDA juice safety regulations.
Asclemed USA Inc. is recalling Dyural-40 Injection Kits because the product insert incorrectly states that the stoppers do not contain latex, when they actually do.
FDA is recalling specific lots of the Covidien Emprint Short Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft during use, potentially remaining in the patient.
Tris Pharma is recalling 19,488 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.
Tris Pharma is recalling specific lots of infants' ibuprofen oral suspension because they may contain a higher concentration of the active ingredient.
Luckyberry is recalling cold-pressed Beetnik juice sold in Lawrence, KS, because the product was manufactured and distributed in violation of FDA regulations requiring pasteurization.
Abbott Point Of Care Inc. is recalling i-STAT CG8+ Cartridges because they may generate inaccurate potassium results, potentially leading to incorrect clinical decisions.