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.
Certain 2022-2023 NOVA BUS LFS vehicles may have missing electrical components that prevent the battery disconnect switch from functioning properly, creating a risk of electrical shock during maintenance.
Kia is recalling 2018-2023 Stinger and 2019-2020 K900 vehicles due to potential engine fire from deteriorating turbocharger oil feed pipes.
Mack Trucks is recalling 2024 Granite vehicles because incorrect Gross Axle Weight Rating labels may allow the vehicles to be overloaded, increasing crash risk.
Winnebago is recalling 2023-2024 Sunstar motorhomes because the tire information label incorrectly states the tire size and Gross Vehicle Weight Rating.
Faraday Future is recalling 2023 FF-91 Alliance vehicles because a software error may prevent the air bag malfunction warning light from illuminating, increasing crash injury risk.
Winnebago is recalling 2024 Solis motorhomes because the lavatory may have a standard outlet instead of a GFCI protected one, increasing the risk of electric shock.
Mack Trucks is recalling 2024 MD6 and MD7 vehicles because the park brake light may display the wrong status, potentially allowing the vehicle to roll away.
Jayco is recalling 2023-2025 Entegra Coach Anthem and Cornerstone motorhomes because foreign material in the steering gear may cause a loss of power steering assist.
Jayco is recalling certain 2021-2024 Solstice LI, Swift, Terrain, Terrain LE, Ethos LI, Expanse LI and Launch LE motorhomes because battery relay contactors may become stuck closed.
Sandford Family 6-Player Croquet Sets are recalled because paint on mallets, hoops, and winning posts contains lead and phthalates at levels that exceed federal bans. Lead and phthalates are toxic if ingested, especially for young children.
BRP is recalling about 8,100 2024 Ski-Doo MXZ and Renegade snowmobiles equipped with Pilot X skis because the left ski can break, creating a risk of serious injury and crash. Consumers should stop using the snowmobiles immediately and contact BRP for a free ski replacement.
Cannondale is recalling 2021–2023 Model Year Dave bicycles because the headtube/downtube weld can become damaged and separate from the frame, creating a fall hazard. No injuries have been reported.
Oso & Me is recalling approximately 170 children's pajama sets that violate federal flammability regulations for sleepwear, posing a burn risk to children. No injuries have been reported.
BMW is recalling R 1300 GS dealer accessory top cases because the locking flap may fail, causing the case to detach and create a road hazard.
Nutraceutical Corporation is recalling Heritage Store Hydrogen Peroxide Mouthwash because the packaging does not comply with child-resistant packaging requirements, posing a poisoning risk if swallowed by young children.
About 720 Liverpool Football Club children's pajamas fail to meet federal flammability standards for sleepwear, posing a burn-injury risk. The pajamas were sold exclusively online from January 2022 through November 2023.
About 1,570 Vanilla Underground "Minecraft TNT" one-piece pajamas fail to meet federal flammability regulations for children's sleepwear, posing a burn injury risk. Consumers should stop using them immediately and contact Vanilla Underground for a refund.
IonoStar Plus dental cement capsules contain an incorrect plunger due to a manufacturing error. The defect prevents proper curing of the cement, making the product unsuitable for use.
Micro Labs Limited is recalling 24,768 bottles of Clobazam 10mg tablets nationwide due to out-of-specification residual solvents. Patients should contact their healthcare provider for guidance.
A framegrabber card malfunction in Philips Allura Xper interventional X-ray systems may cause display failures, preventing proper visualization of medical images and delaying procedures.
Country Corner Dairy is recalling WHITE COLBY CHEESE products due to improper pasteurization. The recalled products were distributed to Maryland and Virginia.
Acthar Gel (repository corticotropin injection) is being recalled due to a temperature excursion during shipping from the manufacturer to distributor. Lot #1564-103 should not be dispensed to patients.
Canon Medical System X-ray C-arm systems may display abnormal images due to an internal board manufacturing defect, potentially preventing exam completion and requiring patients to be re-examined with alternative equipment.
Fortune cookies manufactured by New World Company are being recalled due to undeclared soy allergen. Consumers with soy allergies should not consume the product.
Baxter Healthcare is recalling 13,000 bags of norepinephrine bitartrate injection due to an overwrap label incorrectly showing 4 mg/250 mL concentration, while the primary bag label correctly shows the actual 8 mg/250 mL strength.