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.
Chrysler is recalling certain 2020-2025 Alfa Romeo Giulia and Stelvio vehicles because a defect in the rearview camera system may prevent the camera image from displaying, increasing crash risk. Owners should contact dealers for free inspection and repair.
Lucid is recalling 2022-2025 Air vehicles due to a software defect that may prevent the rearview camera from displaying or show inaccurate images, increasing crash risk. A free over-the-air software update will be provided.
Chrysler is recalling certain 2024–2025 RAM ProMaster battery electric vehicles due to software issues in the electric drive module that may cause loss of drive power, increasing crash risk.
Mack is recalling certain 2019-2025 MD, Anthem, Granite, and 2024 MD Electric and 2025 Pinnacle trucks with passenger bench seats. An improperly welded seat belt anchorage bracket may detach during a crash, increasing injury risk.
USDA FSIS issued a public health alert for FreshRealm ready-to-eat meals containing spinach recalled for possible Listeria contamination. No illnesses have been reported.
REV is recalling 2024-2026 Fleetwood Fortis and Holiday Rambler Invicta RVs with theater seats because theater seat fasteners may have damaged propane hoses, creating a fire hazard.
Hyundai is recalling 2024-2025 Santa Fe vehicles. The starter motor terminal cover may be improperly installed, causing electrical shorts that increase fire risk during crashes.
About 470 Almpal dissolved oxygen test kits are being recalled because the sulfuric acid bottle inside is not in child-resistant packaging, as the Poison Prevention Packaging Act requires.
About 610 Gunaito 10-drawer dressers sold on Walmart.com are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act stability standard.
About 630 Blossom children's two-piece loungewear sets are being recalled because they violate the mandatory flammability standard for children's sleepwear.
About 98,350 Evermore Surprise Eggs are being recalled because the toy airplane inside contains lead above the federal lead content ban. No incidents have been reported.
Philips Brilliance iCT systems, model 728306, are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 210 units are affected.
Extract Labs, Inc. is recalling Elderberry 20mg Gummies (Lot 25JD072107A) due to potential peanut protein cross-contact. Consumers should not use the product if they have a peanut allergy.
Philips Allura Xper FD20 Biplane OR Table systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 5 units are affected.
Extract Labs, Inc. is recalling Mai Tai 20mg gummies due to potential peanut protein cross-contact. The affected product is unlabeled bulk gummies distributed throughout the United States and internationally.
Philips is recalling certain CT systems because the patient support table may descend unexpectedly to the lowest position due to a component misalignment during replacement.
Philips is recalling Brilliance iCT SP CT systems due to a ball screw misalignment that may cause the patient support table to descend unexpectedly to its lowest position.
Sofmed Breathables contact lenses from one lot are recalled because the lot was manufactured with an invalid sterilization cycle. 180 units are affected.
Micronized BPO Gel Cleanser 10% from Pantea MD, 7 oz, lots 58170A and 58172A, is recalled because of elevated levels of benzene. The product was distributed in California and Georgia.
Philips Allura Xper FD20/20 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 75 units are affected.
mel rx Skin NO DRAMA Benzoyl Peroxide 10% Acne Treatment, 7 oz, lots 58170A and 58172A, is recalled because of elevated levels of benzene. The product was distributed in California and Georgia.
Tesla is recalling certain 2026 Model Y vehicles because the reverse lights may fail to illuminate due to a wiring defect, which could reduce visibility when backing and increase crash risk.
Extract Labs Sugar-free Mixed Berry Gummies, lot 25E5082907A, are recalled because of potential peanut protein cross-contact. 2,180 gummies in 109 bottles are affected.
Philips Big Bore RT, Brilliance CT Big Bore Oncology and Brilliance CT Big Bore systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 33 units are affected.
Pure Cane Granulated Sugar in 50 lb bags, distributed by Domino Foods, is recalled because of potential contamination with foreign objects. 4,500 bags are affected.