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.
Tova Industries is recalling Shaver Foods brand Frosting Mix Vanilla due to possible metal shavings in the ingredient. The product was distributed to 11 states and the United Arab Emirates.
Tova Industries is recalling American Bounty brand Icing Mix Vanilla due to possible metal shavings in the ingredient. The recall covers 104 cases distributed to 11 states and the United Arab Emirates.
BMW is recalling 2018-2020 X3 and 2019-2020 X4 vehicles because the instrument panel casing may not be tightened properly, posing an injury risk during air bag deployment.
Cardinal Health is recalling Monoject Hypodermic Safety Needles because they were shipped as non-sterile despite labeling indicating sterility, posing an infection risk.
Tova Industries is recalling Shaver Foods brand Frosting Mix Chocolate Texas due to possible metal shavings in the ingredient.
Cardinal Health 200, LLC is recalling Monoject Bluntfill syringes that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.
Tova Industries is recalling MJ Kellner brand Vegan Soy Based Milk Replacer because of possible metal shavings in the ingredient.
Harris Teeter is recalling Premium Selections Banana Pudding Ice Cream because it contains undeclared soy. Consumers should check their freezers for the affected product.
Medtronic CoreValve LLC is recalling six Simulus 750 Flexible Ring/Band Accessory Kits because demonstration units may have contacted non-human tissue.
The Boyer Corporation is recalling six brands of sodium and potassium hydroxide products because the packaging is not child-resistant, posing a risk of chemical burns.
Thor Motor Coach is recalling 2020 SEQUENCE motorhomes because the transmission shifter cable may separate from the transmission, potentially causing unintended vehicle movement and increased crash risk.
Triumph is recalling 2013-2017 Trophy SE A1 motorcycles because improper brake hose routing may damage ignition wiring, causing engine stalls or lighting loss.
Eldorado National-Kansas is recalling 2017-2019 World Trans vehicles because seat belts may not be properly secured to the side wall, increasing injury risk in a crash.
Nissan is recalling 2020 Infiniti Q60 vehicles because the rear seat belt locking mechanism may fail to lock properly, increasing injury risk in crashes.
BMW is recalling specific 2019-2020 motorcycles because the brake light may flash instead of staying steady during emergency braking, which can confuse other drivers.
Homestar is recalling Finch three-drawer dressers because they can tip over or entrap children if not anchored to the wall.
Jaguar Land Rover is recalling 2017-2018 Discovery vehicles because trailer lights may not function when towing with Daytime Running Lights on, increasing crash risk.
Volvo is recalling 2019-2020 S60, S90, V60, V90, XC40, XC60, and XC90 vehicles because a software issue may prevent the automatic emergency braking system from engaging.
Yamaha is recalling Line 6 Relay G10 wireless guitar systems because the lithium-ion battery can overheat and the cover can separate, posing fire and injury risks.
Kichler Lighting is recalling 52-inch LED ceiling fans because the arms holding the blades can detach, posing an injury risk. No injuries have been reported.
The FDA is recalling 70,361 units of Covidien Force TriVerse Electrosurgical Devices because sterile packaging may be compromised, increasing the risk of infection.
Heartland is recalling 2020 Shadow Cruiser Ultra Lite trailers because certification labels list incorrect GVWR and axle ratings, which could lead to overloading and axle failure.
Beckman Coulter is recalling Direct Bilirubin Reagents because acetaminophen metabolites may interfere with test results, potentially delaying diagnosis and treatment.
Bard Peripheral Vascular Inc is recalling specific lots of Bard Biopsy EnCor Probes due to leaks, suction issues, and failure to obtain samples.
Axia Pharmaceutical is recalling specific lots of Methylcobalamin Injection because the product lacks assurance of sterility. The recall covers distribution in the U.S., Puerto Rico, Barbados, and the Dominican Republic.