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.
Taylor Farms Florida is recalling approximately 732 pounds of chicken salads because they contain undeclared anchovies, a known allergen.
Eldorado is recalling 2017 Axess, Arrivo, XHF, and E-Z Rider II buses because seat belt buckles may be stuck, preventing use.
Indian Motorcycle is recalling 2,096 models from 2017-2018 because some may have European-market headlights that fail US safety standards, increasing crash risk.
Honda is recalling 2,443 2017 CBR1000RR and CBR1000RR SP motorcycles because a gap in the fuel tank cap seal may allow water to enter the tank, potentially causing engine stalling and increasing crash risk.
Jaguar Land Rover is recalling 2017 Range Rover and Range Rover Sport vehicles because the instrument cluster may intermittently go blank, increasing crash risk.
Jaguar is recalling 2016-2018 XF, F-Pace, XJ, and XE vehicles because the instrument cluster may go blank, increasing crash risk.
St. Jude Medical is recalling 1,744 Proclaim DRG Implantable Pulse Generators because the battery indicator status may be inaccurate.
St. Jude Medical is recalling 3,119 Infinity 5 and 7 Implantable Pulse Generators because battery longevity estimations may be inaccurate.
St Jude Medical is recalling 164,366 Assurity MRI pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
Genesys Orthopedics is recalling 120 Binary Screwdrivers because the threaded inner shaft tip can break off during cervical screw insertion.
St. Jude Medical is recalling 10,453 Merlin PCS 3650 programmers worldwide to install new firmware that mitigates the risk of unauthorized access to pacemakers.
St Jude Medical is recalling 2,726 implantable pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
Volkswagen Group of America is recalling 2017-2018 Audi A4 and A5 vehicles because loose aluminum door trim can expose sharp edges, increasing the risk of injury to occupants.
St Jude Medical is recalling 6,051 PM 1260 Assurity+ pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
St Jude Medical is recalling 2,741 Nuance pacemakers to install new firmware that mitigates the risk of unauthorized access to the devices' radio frequency communications.
St. Jude Medical is recalling Merlin@Home software to mitigate the risk of unauthorized access to pacemakers using radio frequency communications.
St. Jude Medical is recalling 28,817 Proclaim 5 and 7 Elite Implantable Pulse Generators because battery longevity estimations may be inaccurate.
St Jude Medical is recalling specific Assurity and Accent pacemaker models to mitigate the risk of unauthorized access via radio frequency communications.
St Jude Medical is recalling 4,828 ZENEX pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
St Jude Medical is recalling specific Anthem and Allure/Relieve pacemakers to mitigate the risk of unauthorized access via radio frequency communications.
USDA FSIS issued a public health alert for Mary's Harvest kale and broccoli slaw salad with chicken due to possible Listeria contamination from a recalled broccoli supplier.
St Jude Medical is recalling 101 implantable pacemaker pulse generators to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.
Diving Unlimited International is recalling approximately 480 scuba diving regulators because they can malfunction, posing a drowning hazard. No injuries have been reported.
CareFusion 303, Inc. is recalling Alaris Pump Module model 8100 units due to reports of increased or decreased medication flows.
Bel Brands USA is recalling Merkts Port Wine Cheese Spread after customers reported finding white plastic pieces in the product.