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.
Bridgestone is recalling specific FS561 trailer tires manufactured in 2015-2016 because tread separation could cause a sudden loss of air pressure and increase crash risk.
Snake River Trailer Company is recalling 2015-2016 Horse Trailers because a weld on the rear axle may fail, causing the wheel assembly to separate and increasing crash risk.
The Noble Spoon is recalling approximately 289 pounds of beef and chicken entrees produced without federal inspection. The products were sold in Marin and Sonoma counties, California.
Stoughton Trailers is recalling 2009-2010 Grain Hopper trailers because a panel may separate, causing cargo to spill or structural failure.
Chrysler is recalling 110,482 vehicles because corroded air bag control units may fail to deploy or deploy unexpectedly, increasing crash risk.
C&B Quality Trailer Works is recalling 2015-2016 horse trailers because a weld on the rear axle may fail, causing the wheel assembly to separate and increasing crash risk.
Volkswagen is recalling 2015 Tiguan and Audi Q5 vehicles because seat-mounted air bag inflators may rupture in a crash, potentially causing serious injury or death.
Chrysler is recalling 2014-2016 Town and Country and Grand Caravan minivans because expired primer may allow the windshield to dislodge in a crash.
Tristar Products is recalling AquaRug shower rugs because the suction cups can fail, causing slips and falls. Consumers should stop using the rugs and contact the company for a free replacement.
Chrysler is recalling 2011-2016 Dodge Chargers because the body-side sill may fail if the vehicle is lifted with the supplied tire jack without chocking the wheels, increasing injury risk.
Ford is recalling 2016 E-350 and E-450 vans with 6.8L engines and trailer brake controllers because the braking system may fail, increasing stopping distance.
RNG Group Inc. is recalling Renogy 100-watt bendable solar panels because they can overheat and cause fires. Consumers should stop using the panels and return them for free replacements.
Arkray Factory USA is recalling specific lots of SPOTCHEM II test strips because they may display inaccurate glucose results for high values.
MWT Materials, Inc. is recalling Accusorb MRI radio frequency shielding blankets and body-part covers because they may overheat and lead to patient injury when not used correctly.
Grato Holdings is recalling Energique Joint Pain & Stiffness Relief Topical Spray due to microbial contamination. Testing revealed out-of-specification results for total aerobic microbiological count.
Home Maid Ravioli Company is recalling approximately 38,950 pounds of meat and poultry ravioli and pasta products due to undeclared allergens and lack of federal inspection.
Pine Pharmaceuticals is recalling Bevacizumab syringes for intravitreal use because they contain silicone oil microdroplets.
Mylan Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.09% because the preservative failed an effectiveness test, raising concerns about sterility.
Amerita Specialty Infusion Services is recalling specific lots of compounded Baclofen syringes because the FDA identified a lack of assurance of sterility.
Grato Holdings, Inc. is recalling 118 bottles of Energique homeopathic skin spray due to out-of-specification microbial counts.
GE Medical Systems is recalling 13 Aisys Anesthesia Systems because a stuck valve could cause excessive pressure in the patient breathing circuit, potentially resulting in barotrauma.
Arkray Factory USA, Inc. is recalling SPOTCHEM II Glucose Reagent Test Strips because a lowered reaction rate causes inaccurate high glucose readings.
MWT Materials, Inc. is recalling Accusorb MRI MAC7010 radio frequency shielding blankets and body-part covers because they may overheat when not used correctly, posing a risk of patient injury.
GE Medical Systems is recalling Aespire 7900 and Aespire View anesthesia systems because a stuck valve could cause excessive pressure and barotrauma.
MWT Materials, Inc. is recalling 49 Accusorb MRI blankets because they may overheat and lead to patient injury when not used correctly.