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.
Michelin is recalling specific BFGoodrich tires because a sidewall rupture in the bead area may cause rapid air loss, increasing the risk of a vehicle crash.
Starcraft RV is recalling 2015-2016 Launch Ultra Lite trailers because improperly secured furnaces may release hazardous exhaust fumes into the cabin.
LGS Industries is recalling 3,612 model year 2015-2016 Look, Pace, and Cargo Express trailers because the coupler latch may not fully lock, risking separation from the tow vehicle.
Viking Range is expanding a recall for about 17,300 dishwashers manufactured before April 2011 because an electrical component can overheat and cause fires.
Forest River is recalling 634 model year 2015-2016 XLR trailers because strained wiring at the external power inlet may loosen and arc, increasing the risk of a vehicle fire.
Rising Sun Farms Inc is recalling Nut Free Pesto due to contamination with Listeria monocytogenes. The product was distributed in Florida and Nevada.
Grand BK Corp. is recalling Goodies By Nature RAW Cashews because of Salmonella contamination. The product was distributed in several states via H Mart stores.
Skeletal Kinetics is recalling 67 kits of InjectionPlasty 1.0 Bone Void Filler due to reports of venous uptake, DVT, and pulmonary embolism in implanted patients.
Draeger Medical is recalling 373 Fabius MRI anesthesia machines because their parts can be loosened by the magnetic field of MRI equipment.
Forest River is recalling 2015 Palomino PaloMini vehicles because axle tube cambers may be installed upside down, increasing crash risk.
Brett Anthony Foods is recalling 8 oz Vegetable Chili containers in Illinois due to undeclared milk, a major food allergen.
New Flyer is recalling specific 2014-2015 NABI transit buses because pressure relief devices may fail to vent gas, increasing the risk of tank explosion, fire, and injury.
Emerson is recalling specific Fisher Pressure Relief Valves used in cargo tank trailers. The valves may restrict flow during a fire, increasing the risk of tank explosion.
Nissan is recalling 46,846 Altima and Maxima vehicles because an improperly installed o-ring may cause fuel to leak during a crash, increasing fire risk.
Volkswagen is recalling specific 2010-2014 models because debris may damage the air bag clock spring, preventing the driver's air bag from deploying in a crash.
Good Food Made Simple is recalling approximately 3,574 pounds of turkey and pork breakfast products that were distributed in California without U.S. inspection.
NVIDIA is recalling approximately 83,000 SHIELD tablet computers because the lithium-ion batteries can overheat and pose a fire hazard.
Greenland Trading Corp. is recalling approximately 12,672 pounds of squab products imported from France without U.S. inspection. The recall addresses a potential risk of adverse health consequences due to the lack of full inspection.
Temsa is recalling 2013-2016 TS45 coaches because low air pressure may cause parking brakes to drag, overheat, and potentially start a fire.
American Medical Systems is recalling 16,710 Sureflex 910 Lithotripsy Fibers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
American Medical Systems is recalling 16,710 Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Philips is recalling 13 GEMINI TF 16 Slice CT/PET systems worldwide due to four software defects in the Tumor LOC application that may affect treatment accuracy.
Philips is recalling 22 GEMINI TF 64 Slice CT/PET systems due to software defects that may cause incorrect tissue irradiation.
Philips is recalling two Gemini LXL CT/PET systems due to software defects that may cause incorrect radiation delivery to patients.
The FDA is recalling 5,786 sterile Double Basin Kits because the included Devon Light Gloves contain splits or holes that compromise sterility.