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.
Ruiz Food Products is recalling approximately 55,013 pounds of frozen breakfast burritos that may contain pieces of plastic. No injuries have been reported.
Bass Pro is recalling MR. STEAK four and five burner gas grills because the fuel line can melt and cause a fire.
Proterra is recalling 2019 Catalyst buses because a software update may have disabled brake interlock warnings, increasing the risk of fire or crash.
ARBOC Specialty Vehicles is recalling 2017-2019 Spirit of Freedom and Spirit of Mobility vehicles because the roof hatch handle may break, preventing emergency egress.
Daimler Trucks North America is recalling 145 school buses due to loose fan hub bolts that could damage components or detach, risking injury during an uncontrolled stop.
Volkswagen is recalling 2013-2015 Jetta Hybrid vehicles because hairline cracks in the transmission can cause oil leaks and sudden loss of drive power, increasing crash risk.
Trek is recalling about 2,840 Super Commuter+ 8S electric bicycles because a front fender bolt can unthread, causing the wheel to detach and posing a fall hazard.
Surly Bikes is recalling about 5,139 front bicycle racks because they can loosen and contact the front wheel, posing crash and injury hazards.
Honda is recalling 2019-2020 CR-V vehicles because improperly manufactured rear subframe bolts may loosen, allowing the subframe to separate and increasing crash risk.
Taher, Inc. is recalling Fresh Seasons Veggie & Ranch Cups because they contain cauliflower potentially contaminated with Listeria monocytogenes.
AuroMedics Pharma LLC is recalling Ranitidine Syrup because N-nitrosodimethylamine (NDMA) has been detected in the product.
AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 300 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
Bentley is recalling 2017-2018 Continental Supersports vehicles because a power steering cooler pipe may be the incorrect size, allowing the hose to detach and leak fluid.
New Vitalis Pharmacy is recalling Testosterone Cypionate and Propionate oil injection solutions due to a lack of sterility assurance.
Zimmer Biomet is recalling Acromium Flange Sets because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a chafing fuel line may cause a leak, increasing the risk of fire.
AVKARE Inc. is recalling specific lots of Ranitidine Tablets 300 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Volkswagen is recalling certain 2011-2015 Golf, Passat, and Audi A3 diesel vehicles because the driver's side air bag inflator may explode.
AuroMedics Pharma LLC is recalling DG Health Acid Reducer Ranitidine Tablets 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
AuroMedics Pharma LLC is recalling MARLIDO KIT vials because foreign material was found inside the vials. The affected product is Lidocaine HCl Injection, USP, 2%.
Preferred Pharmaceuticals is recalling specific lots of Ibuprofen Oral Suspension USP due to the presence of small particles of inert plastic material.
AVKARE Inc. is recalling specific lots of Ranitidine Tablets 150 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
REV Recreation Group is recalling 3,241 Fleetwood and Holiday Rambler motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.