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 has recalled 17,228 MRI systems because the cryogenic ventilation system does not meet safety requirements. Systems were distributed nationwide and internationally.
GE Healthcare has recalled approximately 17,228 MRI systems due to cryogen ventilation systems that may not meet required venting standards. The issue affects systems distributed nationwide and internationally.
GE Healthcare MRI systems may have cryogenic ventilation systems that do not meet venting requirements. The recall affects 17,228 devices distributed nationwide and globally. Healthcare facilities should contact GE Healthcare for corrective actions.
Simply Goodfats Creamy MCT Vanilla MCT Oil Powder is recalled due to undeclared milk allergen. The recall affects approximately 1,647 units distributed online in the US.
GE Healthcare SIGNA HFO/I MR Systems may have cryogen ventilation systems that do not meet venting requirements. Approximately 17,228 systems are affected nationwide and internationally.
BD Veritor Plus Analyzer devices may overheat or catch fire if powered with an unauthorized AC adapter instead of the manufacturer-provided one. The recall affects approximately 129,848 analyzers distributed worldwide.
Gentueri Inc is recalling Viral Transport Medium Kits due to failed sterility testing and evidence of contamination. The recall affects 13,975 units distributed to Illinois, Nebraska, and Wisconsin.
Ford is recalling 2015-2017 Mustangs because loose rearview camera wiring may cause a blank or distorted image, increasing crash risk.
GE Healthcare is recalling MRI systems with potentially non-compliant cryogen ventilation. Over 17,228 superconducting magnetic resonance imaging devices may have cryogen venting systems that fail to meet FDA requirements.
Natural Way Cheese is recalling Cheddar Cheese Curds because milk used in production was stored in a holding tank for longer than the required 72-hour cleaning interval, creating potential for contamination.
The R82 by ETAC Push Brace for High-Low is being recalled because the chrome surface can crack during use, potentially cutting users. Approximately 396 units manufactured between August and October 2021 are affected.
Fuel Helmets is recalling specific SH-WS001 motorcycle helmets that may not adequately protect the wearer in a crash. Owners will receive a credit to replace or reimburse the helmet.
GE Healthcare is recalling 17,228 MRI systems because the cryogen ventilation system may not meet venting requirements. The company is providing field corrections to ensure proper ventilation.
Natural Way Cheese Bacon Cheddar Cheese Curds are being recalled in Michigan and Indiana because milk used in production was stored in a holding tank exceeding the required 72-hour cleaning interval.
Natural Way Cheese is recalling 3 Pepper Cheese Curds (12oz bags) distributed in Michigan and Indiana due to milk stored in a holding tank for more than 72 hours, exceeding required cleaning intervals.
GE Healthcare is recalling 17,228 MRI system magnets with potential cryogen ventilation defects. No injuries have been reported.
Ford is recalling certain 2022 Lincoln Aviator vehicles because the fuel filler tube may detach during a crash, creating a fuel leak and fire risk. Free repairs are available from Ford dealers.
Esme is recalling about 3,600 children's sleepwear garments because they fail federal flammability standards and pose a burn risk. Consumers should stop using them immediately and contact Esme for a free replacement or refund.
GE Healthcare is recalling MR superconducting magnets used in SIGNA Voyager MRI systems due to cryogen ventilation systems that may not meet venting requirements. The recall affects 17,228 devices.
GE Healthcare is recalling 17,228 superconducting magnetic resonance imaging systems due to potential cryogen ventilation system defects that may not meet safety venting requirements.
Lamborghini is recalling 2015-2020 Huracan vehicles because missing caps on headlight adjustment screws can lead to improper alignment, reducing visibility and increasing crash risk.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because incorrect software may cause the airbag warning light to malfunction, potentially masking actual system failures.
Intermotive is recalling 514 Programmable Relay Power Center modules because exposed copper may cause short-circuits, increasing the risk of a fire.
Weldon is recalling specific rear combination lamps because the LED backup lights are the wrong color, failing federal safety standards and potentially affecting vehicle visibility.
Mercedes-Benz is recalling 2021 GLB 250 vehicles because an incorrect front driver's air bag module may not restrain occupants or could detach during a crash.