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.
Altec is recalling certain 2023-2025 Aerial Device and Digger Derrick vehicles because the electronic taillight module harness may have inadequate circuit protection.
Ford is recalling 2022 Transit vehicles where the rearview camera may display a blank image, increasing the risk of a crash while reversing.
General Motors is recalling 2025–2026 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not produce sufficient volume change between stopped and low-speed operation, failing to meet federal safety standards.
About 12,000 JOKOSIS portable bed rails, model HC0262, are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 80 SereneLife above-ground pools 48 inches and taller, models SLPORND15 and SLPORND18, are being recalled because a compression strap may create a foothold allowing a child to access the pool.
About 650 Schwinn Ovation Bicycle Child Carriers are being recalled because the buckles securing the restraints around the child can release during use, posing a fall hazard.
Ford is recalling certain 2021-2022 Bronco vehicles previously repaired under recall 23V165, because the rearview camera image may still be displayed after a backing event has ended.
About 11,200 ANNQUAN power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded.
About 2,800 17 Stories Furniture 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
International Motors is recalling 2026 IC Bus CECB vehicles because wheelchair retractors may fail to lock, increasing injury risk during transit.
About 50,330 jars of Mamisan Pain Relieving Topical Ointment are being recalled because the ointment contains lidocaine and the packaging is not child-resistant.
About 840 bottles of Feel The Beard Minoxidil Beard Growth Oil are being recalled because the product contains minoxidil and the packaging is not child-resistant.
About 260 Currey & Company Electra chandeliers are being recalled because the component connecting the fixture to the ceiling mount is not threaded properly and the fixture can fall.
Bell Sports is recalling Scout Air helmets in sizes S and L because they may lack proper penetration protection, failing federal safety standards.
Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
Medline is recalling 15 Medline Perfusion Syringes because they contain BD Luer Tip Caps from trays that failed routine biocompatibility testing.
Medline is recalling 11,291,800 Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", because packaging may exhibit open seals that could compromise the sterility of the product.
Kia is recalling certain 2023-2025 Sportage and Sportage Plug-In Hybrid vehicles with a 4.2-inch screen and a Kia tow hitch harness, because a software error may make the instrument panel screen fail.
Cipla USA is recalling 15,744 bottles of Cinacalcet Hydrochloride Tablets, 60 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
India's Fine Foods is recalling 10 pieces of 3 B Cookware, UPC 0884964120154, over potential contamination due to leachable lead.
Medline is recalling 6,989,900 Quick Strip Fabric Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.
Bard Peripheral Vascular is recalling 1,240 Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator can show the catheter in the sharp position when it is blunt.
Medline is recalling 18,000 units of Curad Quick Strip Fabric Bandages because packaging may exhibit open seals that could compromise the sterility of the product.
JR Simplot is recalling 7,053 cases of Simplot Traditional Reduced Sodium Tater Gems after pieces of semi-rigid plastic were found embedded in the product.
Cipla USA is recalling 12,576 bottles of Cinacalcet Hydrochloride Tablets, 90 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.