Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
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.
Supreme is recalling 2015-2016 Classic American Trolley vehicles because their windshields do not meet federal safety standards, potentially reducing driver visibility.
Crossroads RV is recalling 2016 ReZerve travel trailers because the Federal Identification Label incorrectly states the axle capacity, potentially leading to overloading and loss of control.
Tesla is recalling 2012-2015 Model S vehicles because front seat belts may be improperly connected to the pretensioner, increasing injury risk in a crash.
BMW is recalling 2015-2016 Rolls-Royce Phantom vehicles because side curtain air bags may not deploy correctly, increasing injury risk in crashes.
Suzuki is recalling 600 model year 2016 GSX-S1000, GSX-S1000A, and GSX-S1000FA motorcycles because front brake calipers may leak fluid, reducing braking performance.
Nissan is recalling 2015 Rogue vehicles because the shift selector knob may allow shifting out of Park without depressing the brake pedal, increasing the risk of a crash.
Isuzu is recalling 2012-2016 NPR, NQR, and NRR trucks because the installed fire extinguishers may fail to discharge. Owners should contact Isuzu or Kidde for a free replacement.
New England Wheels is recalling 2006-2014 Ford E-250 and E-350 vans with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure the operator.
Polaris is recalling 2015-2016 Slingshot motorcycles because a headlight relay may fail, causing loss of headlights and increasing crash risk.
Amax is recalling Bostitch electric pencil sharpeners because internal components can energize the unit, posing a shock hazard. One consumer reported receiving a shock.
Micro Bird is recalling 2006-2014 transit buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.
Coach and Equipment is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts. The lifts may have pivot holes that allow bearings to move, risking platform failure.
Forest River is recalling specific 2012-2016 recreational vehicles because a water heater valve may cause overheating, potentially leading to steam release and scalding injuries.
Gillig is recalling Ricon Model S5510 wheelchair lifts because oversized pivot holes may allow bearings to shift, potentially causing the platform to fall and injure the operator.
Nation Pizza is recalling approximately 59,028 pounds of frozen Mama Cozzis Pizza Kitchen products because they contain undeclared soy, a known allergen.
Kingmor is recalling 271 IC CE school buses equipped with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure operators.
Forest River is recalling 2006-2014 Glaval buses equipped with specific Ricon wheelchair lifts due to a defect that could cause the platform to fall.
Shimadzu Medical Systems is recalling 26 C-arm Tables because the C-arm may interfere with the table top under certain circumstances.
GE Healthcare is recalling 756 MRI scanners because displayed SAR values may be lower than actual head SAR, potentially exceeding safety limits during head or neck scans.
GE Healthcare is recalling 19 Signa 3.0T MRI systems because displayed SAR values may be lower than actual head SAR, potentially exceeding safety limits.
Teleflex Medical is recalling Rusch Flexi-slip tracheal tube stylets because the plastic coating may split or break off.
Stryker Howmedica Osteonics Corp. is recalling 201 Vitallium femoral heads because they could not be assembled with their corresponding stems during surgery.
Miramar Labs is recalling 277 miraDry Systems to update labeling that reminds users to use only approved lubricants in a thin layer to prevent burns and blisters.
NeuroLogica Corporation is recalling seven Samsung GM60A-40S radiographic systems because drive behavior may not be properly controlled when moving over conductive floors.
Bonduelle USA Inc is recalling specific lots of frozen corn found to be contaminated with Listeria monocytogenes. The recall includes precautionary lots produced on the same day as the suspect product.