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.
English Riding Supply is recalling about 49,300 Ovation Protégé equestrian helmets because they fail to meet safety impact standards. Riders who fall face an injury risk.
BRP is recalling about 3,310 Model Year 2023 Can-Am side-by-side vehicles because a defective fuel hose assembly could leak fuel and create a fire hazard. Consumers should stop using the vehicles and contact a Can-Am dealer for a free repair.
Skip Hop is recalling Silver Lining Cloud Activity Gyms because raindrops attached to the included cloud toy can detach and pose a choking hazard to children. No injuries have been reported.
Chamberlain Group is recalling about 96,400 LiftMaster myQ garage door control panels because the secondary entrapment protection system can fail, allowing the garage door to close even when an obstruction is present. No injuries have been reported in the U.S.
Daimler Trucks North America is recalling 2021-2023 Freightliner Coronado vehicles because upper bunk mounting bolts may loosen, posing an injury risk.
IKEA is recalling about 12,000 ODGER Swivel Chairs in anthracite because the leg base can break, creating a fall hazard. Four reports of leg base breaking have been received, including two reports of consumer injuries from falls.
Forest River is recalling certain 2022-2023 Coachmen motorhomes with faulty cooktops. The burner tubes may fracture and leak gas, creating a fire hazard.
Textron Specialized Vehicles is recalling about 143,000 E-Z-GO personal transportation vehicles because the electronic board powering the USB port can overheat and ignite, creating a fire hazard. Consumers should stop using the vehicles immediately and contact Textron for a free repair.
Chrysler is recalling specific Mopar Trailer Reverse Steering Control Modules because they may prevent the rearview image from displaying in reverse, increasing crash risk.
Chrysler is recalling 2021–2023 RAM 2500, 3500, 4500, and 5500 Cummins diesel trucks due to an electrical short in the heater grid relay that can cause engine compartment fires. Owners should park outside and away from structures until repairs are completed.
Certain 2021-2023 RAM 1500 and 2023 RAM 2500 vehicles have a software defect that may prevent the rearview image from displaying when in reverse, reducing driver visibility.
Medline Industries recalls non-sterile procedural trays (LAPAROTOMY CDS) because sterile blades within the kits may puncture the outer foil packaging, compromising sterility.
Ameripack Foods LLC is recalling Chocolate Chunk Brownies (UPC 4122077413) due to undeclared soy and egg allergens. Consumers with allergies to these ingredients should not consume the product.
Alpha Plant-Based Burrito products contain undeclared milk that poses an allergen risk. THE MISO BROTHERS INC is recalling 31,092 units distributed throughout US retail locations.
Certain Siemens fluoroscopic X-ray systems may only boot into backup mode after an abrupt shutdown, preventing full operation. This could necessitate cancelling or switching to alternative treatment systems.
Medline Industries is recalling 420 units of UNITE FOOT & ANKLE Screws nationwide due to observed intra-operative screw failure when used with specific drill bit sizes. The failure occurs due to excessive torque during surgical insertion.
Medline Industries recalls non-sterile Total Knee procedural trays because sterile blades inside can puncture the outer foil packaging. This could compromise sterile blade integrity.
The Miso Brothers is recalling Alpha Plant Based Breakfast Burritos because they contain undeclared milk. This poses a risk to consumers with milk allergies or sensitivities.
THE MISO BROTHERS INC is recalling Alpha Plant-Based Burrito - CHIK'N FAJTA frozen breakfast burritos because they contain undeclared milk that is not listed on the label. The product poses a risk to consumers with milk allergies.
Medtronic Perfusion Systems is recalling 1,340 units of the Affinity Fusion Oxygenator due to reports that the Temperature Monitoring Adapter can come loose during or after use in cardiopulmonary bypass procedures.
Medline Industries is recalling 45 units of procedural trays containing sterile surgical blades. The sharp blades may puncture the outer sterile packaging, potentially compromising sterility and increasing infection risk.
Medline Industries recalls non-sterile orthopedic procedural trays that may contain sterile blades capable of puncturing the protective foil packaging, compromising sterile barriers.
Medtronic is recalling Affinity Fusion Oxygenators because the Temperature Monitoring Adapter may come loose during setup or disassembly of the heart-lung machine used in cardiac surgery. No injuries have been reported.
Biomet is recalling certain OSS Modular Arthrodesis Nails due to missing locking bolts that could require extended surgery. Affected units are Lot 136620.
THE MISO BROTHERS INC is recalling Alpha Plant-Based Burritos because they contain undeclared milk, a common allergen. Approximately 31,092 units are affected across US retail locations.