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.
R&M Trailer is recalling 185 model year 2012-2013 enclosed cargo trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.
GE Healthcare is recalling Panda iRes and Freestanding Infant Warmers because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture delivered to patients.
B. Braun Medical is recalling AccuFlo Elastomeric Infusion Pumps because internal testing found flow rates outside specifications, which may cause overly rapid medication infusion.
Elekta, Inc. is recalling 1,424 XiO RTP Systems because the software may calculate incorrect Effective Depth values when bolus is present.
GE Healthcare is recalling Precision 500D, MPI, and RXI X-ray systems because a locking nut on the overhead monitor suspension may loosen.
GE Healthcare is recalling 1,970 Giraffe Infant Warmers because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture delivered to patients.
GE Healthcare is recalling 375 Stand-Alone Resuscitation T-Pieces because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture delivered to patients.
Siemens Medical Solutions is recalling 147 SOMATOM CT systems due to a potential display freeze malfunction during clinical operation.
Prime Snax Inc. is recalling approximately 90,000 pounds of beef jerky products because they contain soy lecithin, a known allergen not declared on the label.
Midway Specialty Vehicles is recalling 21 model year 2010 Pinnacle buses because voltage spikes may damage door actuators, increasing the risk of a fire.
Yamaha is recalling 2009-2013 YZFR1 and 2012-2013 XTZ12 motorcycles because headlight sockets may overheat and melt, causing headlight failure and increasing crash risk.
Graco is recalling approximately 4.2 million toddler and booster seats because the harness buckle may get stuck, making it difficult to remove a child in an emergency.
Trailers USA is recalling 2013 horse trailers with Fastec door locks that may jam, potentially trapping occupants inside.
Pepe Ganga Corp. is recalling 100 Musical Christmas lights sold in Puerto Rico due to fire and shock hazards. No injuries have been reported.
Starcraft is recalling 2014 Launch travel trailers with incorrect tire size labels. The error may lead to improper tire installation and increased crash risk.
Toyota is recalling 2014 Highlanders because the third-row middle seat belt may not be properly secured to the vehicle floor, increasing injury risk in a crash.
BebeLove is recalling about 3,600 baby walkers due to fall and entrapment hazards. Consumers should stop using them immediately and contact the company for a free repair kit.
Synergetics Inc is recalling 96 units of 25ga Endo Illuminator devices because faulty seals on the outer pouch could fail, potentially compromising sterility.
Synergetics is recalling 25ga Aspirating Endo Illuminators because faulty seals on the outer pouch could fail, compromising the sterile status of the ophthalmic devices.
American Importing Co. is recalling Target Simply Balanced Herb Mixed Freeze Dried Vegetables due to a potential for undeclared soy.
Synergetics Inc. is recalling 36 units of 25ga Awh Chandeliers because faulty seals on the outer pouch could fail, compromising the sterile status of the ophthalmic devices.
Synergetics Inc is recalling 48 units of Stiff 25ga Endo Illuminators because faulty seals on the outer pouch could result in seal failure.
Synergetics Inc. is recalling specific lots of Corona Shielded Wide Field Endo Illuminators because faulty seals on the outer pouch could fail, compromising sterility.
The Lambs Farm, Inc. is recalling Banana Nut Bread loaves sold in Bread Trio gift boxes because the labels do not declare soy allergens.
Synergetics Inc. is recalling 233 units of 29ga Oshima Dual Chandeliers because faulty seals on the outer pouch could fail, compromising the sterile status of the devices.