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.
Bentley is recalling one 2020 Flying Spur because the fuel tank may not have been welded properly, creating a risk of fuel leak and fire.
Spartan Fire is recalling 2019-2021 Gladiator and Metrostar vehicles because steering gear mounting bolts may loosen, causing difficulty steering.
GLG Trading Inc. is recalling approximately 96,810 pounds of beef tallow hotpot seasoning imported from China without FSIS inspection. No adverse reactions have been reported.
KME is recalling 2001-2020 TDA tractor-drawn aerial firetrucks because incorrect wiring in the trailer's ABS control module may cause brake failure, increasing crash risk.
E-One is recalling 2020 Typhoon, Typhoon N, and Cyclone II vehicles because steering gear mounting bolts may loosen, causing difficulty steering.
AH Company International Distribution is recalling approximately 30,081 pounds of Monique Ranou pork pâté products imported without FSIS re-inspection.
KME is recalling certain Predator fire trucks because rear axle welds may be insufficient, potentially causing loss of vehicle control and increasing crash risk.
Cooper Tire is recalling specific Discoverer, Evolution, and other brand tires because the sidewall may bulge or separate, potentially causing a rapid deflation and crash.
Ford is recalling certain 2020-2021 F-150 and Super Duty trucks because the windshield may not be properly bonded, risking detachment in a crash. Dealers will remove and reinstall the windshield at no cost.
Trail King is recalling 2021 TKSA trailers because a cross member in the slide pan frame may crack and detach, increasing crash risk.
Ducati is recalling 2016-2018 XDiavel motorcycles because the side stand bracket may fail, causing the bike to fall and potentially injure nearby persons.
Boston Scientific is recalling 1,953 EMBLEM S-ICD Model A209 devices because electrical overstress may cause malfunction. The devices were distributed in the US and worldwide.
Apotex Corp. is recalling Enoxaparin Sodium Injection syringes because some barrels may display incorrect strength markings.
Cummins is recalling certain Westport B6.7N natural gas engines because incorrect software calibration may prevent the engine from limiting speed or torque, potentially compromising safety functions like braking and stability control.
Newmar is recalling 2017–2021 Dutch Star and 2021 Kountry Star motorhomes because the brake light switch may chafe against the windshield wiper mechanism, preventing brake lights from illuminating. This increases crash risk.
Aomori Olympus is recalling SD-240U-25 electrosurgical snares because inspection found some sterile packages have inadequate seals, posing an infection risk.
Boston Scientific is recalling 872 Emblem MRI S-ICD Model A219 devices because electrical overstress may lead to device malfunction.
Argon Medical Devices is recalling 1,759 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.
Argon Medical Devices is recalling the TLAB Transjugular Liver Biopsy System because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.
Stanley Specialty Pharmacy is recalling Lidocaine/Tetracaine ointment because the lidocaine concentration is higher than listed on the label.
EVR Foods Inc. is recalling LAVVA Blueberry Dairy Free Pili Nut Yogurt because the product may contain mold. The recall covers 806 cases distributed across 14 states.
Cook Inc. is recalling 42 units of Kwart Retro-Inject Ureteral Stent Sets because they were manufactured with incorrect material, which may cause the stent to be stiffer and susceptible to degradation, breakage, or fragmentation.
Ford is recalling 2004-2006 Ranger vehicles because certain replacement air bag inflators may explode during deployment, potentially causing serious injury or death.
Argon Medical Devices is recalling 863 TLAB Transjugular Liver Biopsy Systems due to a manufacturing error that may cause the sheath to separate during use.
World Finer Foods is recalling Reese Hollandaise Sauce in 7.5 oz glass jars due to compromised vacuum seals and product expansion that may allow microorganism growth.