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.
Forest River is recalling 2017-2019 Shasta Revere SHT32FE recreational trailers because the liquid propane gas line may be improperly installed, posing a fire risk.
Airstream is recalling 2017-2020 Basecamp trailers because the tire placard lacks spare tire information, which may lead to installing the wrong size tire.
BMW is recalling 2019 X7 xDrive40i and xDrive50i vehicles because the driver and passenger head air bags may not be properly aligned, potentially impairing deployment and increasing injury risk.
General Motors is recalling 2016-2019 Chevrolet Express and GMC Savana vehicles because rear-quarter windows may use tempered glass instead of laminated glass, increasing injury risk in crashes.
Jaguar Land Rover is recalling 28,671 2016 Range Rover and Range Rover Sport vehicles because a stuck spring may leave the left door unlatched, increasing crash risk.
DICK'S Sporting Goods is recalling Ethos Pull-Up Assist equipment because a plastic clip can break, posing a laceration hazard. Seven reports of equipment breaking resulted in six lacerations.
Revelate Designs is recalling 2019 Terrapin System 14L bicycle seat bags because straps can detach and entangle in the rear wheel, posing crash and injury risks.
Audi is recalling 2016-2018 Q3 vehicles with LED headlights because a broken front turn signal may not alert the driver, increasing crash risk.
Far East Brokers is recalling Fabulous Home Pineapple Corer & Slicers because the metal blade can detach, posing a laceration hazard.
Terumo is recalling 1,258 Electronic Patient Gas Systems because a flowmeter defect may cause inaccurate gas flow rate output.
Pentax of America Inc is recalling 68 C2 CryoBalloon Pear Focal Catheters because incorrect default doses and increments may be transmitted to the controller if the RFID tag is not correctly readable.
Philips is recalling SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Abbott Ireland Diagnostics Division is recalling Alinity i Estradiol Reagent Kits because patient results may be falsely elevated for individuals treated with Mifepristone.
Philips is recalling SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Becton Dickinson is recalling 124 BD Veritor System Readers due to background calibration issues that may cause false positive or negative test results.
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 100 sterile pouches because a cut or hole may compromise the product's sterility.
Philips is recalling SureSigns VS3 patient monitors because a software defect prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Siemens is recalling 459 Artis Zee angiography systems because the floating tabletop movement may be blocked after a collision sensor is activated.
AmeriHerb International Inc is recalling 256 lbs of parsley flakes potentially contaminated with E. coli. The product was distributed nationwide and to Canada.
Becton Dickinson & Co. is recalling 32 BD Veritor Plus Analyzers because background calibration issues may cause false positive or negative test results.
Siemens is recalling 459 Artis Zeego angiography systems because the floating tabletop movement may be blocked after a collision sensor activates.
Shippert Medical Technologies is recalling Tissu-Trans Syringe Fill 360 devices because the sterile pouch integrity cannot be assured without visual examination.
Pentax of America Inc is recalling 157 C2 CryoBalloon Standard Focal Catheters because incorrect default doses and increments may be transmitted to the controller if the RFID tag is not correctly readable.
Shippert Medical Technologies is voluntarily recalling 6,553 units of Tissu-Trans FILTRON 1000 sterile, disposable, one-patient use devices due to a Class II safety concern.
Stanley Security Solutions is recalling 1,101 M200 Fall Monitoring Systems due to a damaged capacitor on the printed circuit board.