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.
International is recalling certain 2026-2027 MV vehicles because the ECU software may fail to engage the brakes when adaptive cruise control or hill hold assist is in use.
About 11,000 3-Pack Smoke Detector Fire Alarms are being recalled because if the sensing threshold is set too high, the alarm might not sound in a timely manner.
About 550 Fortemotus-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 590 CheerKid baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
About 800 Beloems-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
GM is recalling certain 2024 Cadillac Lyriq vehicles because the rearview camera screen may turn gray with no camera image.
About 1,200 Colombia-themed magnetic board games are being recalled because the magnetic game pieces contain loose high-powered magnets, posing an ingestion hazard to children.
About 32,900 hydromassage rotary jets in Highlife Collection spas are being recalled because the suction force can entangle a user's hair and submerge their head underwater.
About 166 SOOWERY 6-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.
Diva Fam is recalling Sea Moss Gel Superfood in the Lemon Pie flavour over potential Clostridium botulinum contamination.
Rich Products is recalling 2,792 cases of Gluten Free 14" Seasoned Vegan Pizza Crust because the product contains undeclared milk and egg.
Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.
Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.
Focalyx Technologies is recalling 18 units of Focalyx Fusion because accessories may not function properly with Windows 10, which may cause patient harm during biopsy or delay treatment.
FUJIFILM Healthcare Americas is recalling 16 FDR Visionary Suite systems because welded contactor contacts may keep supplying current after the device is switched off.
Beckman Coulter is recalling 50 CellMek SPS Sample Preparation Systems because a software error dispenses samples close to or touching tube bottoms, removing 60-100 microliters from the final sample.
Fujirebio Diagnostics is recalling 23 units of Lumipulse G pTau217/beta-Amyloid 1-42 Plasma Ratio because falsely elevated ratio results can incorrectly classify a patient as having amyloid pathology.
Triumph is recalling certain 2022-2024 Bonneville, Street Twin, Street Scrambler, Speed Twin 900 and Scrambler 900 motorcycles because the wiring between the alternator and main harness connector may short circuit.
Imu-Tek Animal Health is recalling 113 bottles of Imu-Tek Immuno-5 Colostrum Powder, 7 oz, over an undeclared milk allergen.
CS Beef Packers is recalling approximately 22,912 pounds of raw ground beef products that may be contaminated with E. coli O145. The products were distributed to foodservice locations in California, Idaho, and Oregon.
Diva Fam is recalling Sea Moss Gel Superfood in the Passion Fruit flavour over potential Clostridium botulinum contamination.
Beacon Promotions is recalling 5,788 units of repackaged M&Ms candies, 1.3 oz, over undeclared milk, soy and peanut allergens.
Changchun Wancheng Bio-Electron is recalling 1,000 units covering the Male Fertility Sperm Test for Home Use (Cassette) because tests requiring a 510(k) were distributed before they could be legally marketed.
Changchun Wancheng Bio-Electron is recalling 91,366 units of LotFancy Urinary Tract Infection Urine (UTI) Test Strips because tests requiring a 510(k) were distributed before they could be legally marketed.
Changchun Wancheng Bio-Electron is recalling 500 units of the Vivoo pH Test because tests requiring a 510(k) were distributed before they could be legally marketed.