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.
GE Healthcare is recalling 42 Discovery MI CT systems installed with a specific electrical panel that may not be properly wired to the UPS.
Siemens Medical Solutions USA is recalling SOMATOM Perspective 16 CT scanners due to a software issue that may cause unnecessary radiation exposure.
Griffith Labs U.S.A. is recalling 183 bags of Seasoned Crouton Seasoning N5 due to the potential presence of Salmonella from a recalled whey ingredient.
Mondelez Global is recalling Ritz Bits Cheese Big Bags because a supplier's whey powder ingredient may contain Salmonella.
Griffith Labs U.S.A. is recalling 50-pound bags of Romano Garlic Seasoning due to potential Salmonella contamination from a recalled whey ingredient.
NEMO Equipment is recalling about 7,500 Stargaze recliner chairs because plastic joint supports can break, posing a fall hazard.
Micro Bird is recalling 2015-2018 G5, MB II, and T-Series transit buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in crashes.
Garden State Bus Group is recalling 2015 Double Deck Buses because the roof emergency exit is incorrectly located, potentially delaying evacuation during an emergency.
Hale Products Inc is recalling Kubota Diesel Powered Portable Pumps because improper wiring may prevent warning lamps from illuminating, increasing the risk of injury if the engine fails.
Micro Bird is recalling 2015-2018 G5, MB II, and T-Series school buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in a crash.
Newmar is recalling 2018-2019 motorhomes because improperly adjusted door latch rods may allow the entry door to open during transit.
Mercedes-Benz is recalling 2018 CLA250 and CLA45 AMG vehicles because the front passenger air bag may fail to deactivate if a child seat is installed.
Mercedes-Benz is recalling 2018 E-Class and 2019 CLS vehicles because the front passenger air bag may not deactivate if a child seat is installed, increasing injury risk.
Honda is recalling Genuine Accessory Centerstand Kits for 2016-2018 Africa Twin motorcycles because a broken circlip can cause the stand to detach, creating a road hazard or causing the bike to fall.
Mercedes-Benz is recalling 2018 GLE 350 and AMG GLE43 vehicles because the panoramic sunroof may not be properly adhered, creating a road hazard.
Thor Motor Coach is recalling 2017-2019 Aria and Venetian motorhomes because brake caliper mounting bolts may loosen, potentially reducing braking performance.
Miller Fireworks is recalling specific rocket and cracker fireworks that violate federal standards due to explosion and burn hazards.
General Motors is recalling 2018 Chevrolet Express and GMC Savana vans because the tire pressure monitoring system may be incorrectly calibrated, potentially delaying low-pressure warnings.
CPSC recalls Hill Topper electric bike motor controllers that may accelerate on their own, posing crash and injury risks to riders.
Textron Specialized Vehicles is recalling about 255 Arctic Cat snowmobiles because the handgrip can break, posing an injury hazard to the rider.
DePuy Orthopaedics is recalling two lots of CORAIL femoral stems labeled as Size 11 but actually Size 12 due to fit and mechanical risks.
Philips Healthcare is recalling 459 Allura Xper systems because shutter positions reset when procedure types change, potentially affecting imaging accuracy.
Siemens is recalling six AXIOM Artis angiography systems in the US due to a defective sealing that could allow coolant to leak into electrical parts.
Implantcast GmbH is recalling specific 2M insert 15degree orthopedic hip implant components because the retaining ring may be incorrectly mounted.
Life Technologies is recalling Gibco CTS OpTmizer T Cell Expansion Serum Free Medium due to compromised fill port tube seals that may allow mold growth.