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.
Southern Classic Food Group LLC is recalling Milo's Sauce in 5-gallon pails due to undeclared fish allergen. Consumers with fish allergies should not consume the affected product.
Firebird Artisan Mills Gluten Free Organic Brown Rice Flour (50 lb bags, Lot #F21-00198) is recalled due to potential Salmonella contamination. The affected product was distributed to CA, IA, IL, and NY.
Medtronic is recalling 67,339 CoreValve Evolut PRO Delivery Catheter Systems manufactured before July 11, 2020, due to reports of actuator separation that could affect device function.
Boston Scientific is recalling six Essentio pacemaker models due to a hydrogen release defect that may compromise a critical capacitor and cause accelerated battery depletion. Approximately 31,548 units worldwide are affected.
Boston Scientific is recalling Accolade pacemaker models L300, L301, L310, L311, L321, and L331 due to latent hydrogen release that compromises the capacitor and accelerates battery depletion.
Cardinal Health is recalling Nonsterile Femoral Angiography and Cesarean Birth Drapes (15,360 units) because plastic film causes sticking that may prevent proper unfolding and application.
Beechnut Nutrition is recalling Beech-Nut brand Single Grain Rice Baby Cereal because certain lots may contain inorganic arsenic above safe levels. Consumers with affected products should stop use and contact the manufacturer.
Micro Bird is recalling 2003-2022 school buses because the service door emergency release handle may bind, preventing evacuation in an emergency.
Micro Bird is recalling 1,323 transit buses because the service door emergency release handle may bind, preventing evacuation in an emergency.
Summit Bodyworks is recalling one 2017 Freightliner M2-106 because its rear LED lights are too bright, potentially blinding other drivers and increasing crash risk.
Fuel may leak at a pipe connection in affected 2021-2022 Hyundai Santa Fe and Sonata vehicles with 2.5L engines, increasing fire risk.
Nissan is recalling 2021 Rogue Sport vehicles because liftgate hinges may separate during rear-end crashes, compromising door retention. Dealers will replace the hinges free of charge.
General Motors is recalling certain 2022 Chevrolet Bolt EV and Bolt EUV vehicles because driver-side air bag fasteners may be missing or improperly tightened. This could prevent the air bag from deploying properly in a crash.
Kia is recalling 2022 K5 vehicles with 2.5L turbocharged engines due to fuel leaks that increase fire risk. Dealers will repair the fuel pipe at no cost.
Canyon Furniture has recalled about 1,200 Creekside Kids Five-Drawer Chests sold at Rooms To Go because the chests are unstable without wall anchoring and pose tip-over and entrapment hazards to children.
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter, Metris, and Freightliner Sprinter vehicles because seat belt retractors may deactivate early, preventing child restraints from securing properly.
One lot of PORTEX ULTRperc Percutaneous Dilation Tracheostomy Kit (Lot 4072715) was incorrectly labeled as 7.0mm when it is 9.0mm. The 40 units were distributed in Pennsylvania, Michigan, Maryland, and Florida.
Philips is recalling 1,301 monitor bracket assemblies used with CT systems due to shaft wear that could cause monitors to fall, potentially injuring patients, operators, bystanders, or service personnel.
Philips CT fluoroscopy monitors may develop bracket shaft wear that could lead to the monitor detaching and falling while attached to cables.
Cuisine Solutions is recalling JUST Egg Inspired by Mexico Roasted Poblanos Sous Vide Plant Egg Bites nationwide due to undeclared egg and milk allergens. Consumers with allergies to egg or milk who purchased these products should not consume them.
Synaptive Medical is recalling 1,291 Trackable Suction Sets for visible metal burrs and filings along the inner suction tube. The defect may contaminate the surgical field or cause injury.
SPINEART SA is recalling 44 units of PERLA TL Lateral Connector Open spinal fusion connectors distributed in the U.S. due to external labels that incorrectly list the rod size.
Philips is recalling 1,301 Monitor Bracket Assemblies used in CT and PET/CT imaging systems worldwide due to potential shaft wear that could cause the monitor to detach from the ceiling mount and fall, posing injury risk.
Edwards Lifesciences is recalling 990 units of the Edwards TruWave (30 cc)/VAMP Jr Kit pressure monitoring set because the pressure tubing may detach from the blood sampling system. Healthcare facilities should discontinue use.
Philips is recalling 1,301 monitor bracket assemblies for CT imaging systems due to shaft wear that could cause detachment and fall of the monitor. This could result in serious injury to patients, operators, and staff.