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.
North Country Smokehouse is recalling approximately 9,000 pounds of pork banger sausage because the product contains wheat despite a gluten-free claim.
Forest River is recalling 2018-2019 Surveyor trailers because the Federal Placard lists 3,500 lb axles instead of the actual 2,500 lb capacity, risking overload and loss of control.
Gillig is recalling 2014-2019 Low Floor buses because uncovered electrical terminals in the headlight circuit may short circuit, causing a loss of headlights and increasing crash risk.
Forest River is recalling 2019 Georgetown motorhomes because the front overhead bunk latch board may fall while driving, increasing injury risk.
TJX is recalling Aroma Home USB Heated Hottie heating pads sold at T.J. Maxx and Marshalls because they can overheat, posing fire and burn risks.
Dexter Axle is recalling specific axle models because they may lack proper grease on inner and outer bearings, which could cause wheel lockup and increase crash risk.
Kovatch Mobile Equipment is recalling 2018 Predator TDA vehicles because a weld on the waterway pipes may fail, causing pipes to detach and injure nearby people.
General Motors is recalling 2019 Chevrolet Equinox and GMC Terrain vehicles because insufficient welds on the rear-right seat head-restraint bracket may increase injury risk in a crash.
Philips is recalling Ingenia 3.0T CX MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Achieva 7.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that could cause leaks and reduced drug delivery.
Highland Ridge RV is recalling 74 units of 2019 Mesa Ridge and Open Range Ultra Lite travel trailers because the weight label exceeds the safety chain rating.
Arrow International Inc. is recalling specific Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.
Gilda Industries is recalling Panque Butter Pound Cake because the product fails to declare milk as an ingredient. The recall covers specific lots distributed to domestic consignees.
Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.
Arrow International is recalling 26 units of the AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.
Philips is recalling MARLIN 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Ingenia Ambition S MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Arrow International is recalling 8 units of the AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.
Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.
Philips is recalling 11,226 Intera 0.5T MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling 11,226 Ingenia Ambition X MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Cardinal Health is recalling Curity All Purpose Sponges because they were not sterilized. The affected units were distributed in the US, Canada, and Colombia.