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.
General Motors is recalling 2015 Cadillac Escalade and Escalade ESV vehicles because a manufacturing defect may cause inconsistent passenger air bag deployment.
Micro Bird is recalling 2006-2014 school buses equipped with specific Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.
Spartan is recalling 2006-2013 emergency vehicles because a failing transmission fluid cooler may allow engine coolant to mix with transmission fluid, increasing crash risk.
Sam Kane Beef Processors is recalling approximately 90,987 pounds of ground beef products due to possible contamination with extraneous materials, including metal.
Land Rover is recalling 28,037 vehicles because the tire pressure monitoring system may fail to detect low pressure, increasing crash risk.
New England Wheels is recalling 2006-2014 Ford E-250 and E-350 vans with specific Ricon wheelchair lifts because the platform side plate may crack.
PACCAR is recalling Eaton V2020 Vane Pumps because the shafts could break, causing pump failure and a sudden loss of power steering assist.
Toys R Us is recalling Koala children's sandals because the butterfly wings can detach, posing a choking hazard to young children.
Zazou Scarves is recalling about 3,800 women's silk scarves because they fail to meet federal flammability standards, posing a risk of burn injury.
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during attachment or manipulation.
Supreme Distributors is recalling Supreme Choice brand crab meat due to potential Clostridium botulinum toxin formation from temperature abuse.
Peters Surgical is recalling 4,976 units of CARDIOXYL synthetic surgical sutures because a potential splitting of the surface treatment on thread ends was identified.
Supreme Distributors, Inc. is recalling Supreme Choice brand crab meat due to potential Clostridium botulinum toxin formation from temperature abuse.
Philips Medical Systems is recalling 61 CT scanners because the Extended Display Field of View reconstruction feature produces inaccurate CT numbers and anatomy.
Supreme Distributors is recalling 16 oz cans of Colossal Crab Meat due to potential Clostridium botulinum toxin formation from temperature abuse.
Roots Organic Gourmet is recalling Thai Coconut Curry Hummus because the label lists Tamari but lacks a 'Contains Soy' statement.
Roots Organic Gourmet is recalling Original Hummus because the label fails to state 'Contains Soy' despite listing Tamari as an ingredient.
Supreme Distributors is recalling 16 oz cans of Special Crab Meat due to a potential risk of Clostridium botulinum toxin formation from temperature abuse.
Vapotherm is recalling 22,042 Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
Supreme Distributors, Inc. is recalling Supreme Choice brand Premium Pasteurized Crab Meat due to potential Clostridium botulinum toxin formation from temperature abuse.
Roots Organic Gourmet is recalling Lima Bean Hummus because the label lists Tamari but fails to state 'Contains Soy.'
CareFusion is recalling approximately 318,280 heated infant breathing circuits due to a regulatory compliance risk involving a material change to the gas pathway.
Vapotherm, Inc. is recalling 1,005 units of Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
Siemens is recalling 206 Artis zee and Artis zeego X-ray systems because radiation release can become blocked unnecessarily under certain circumstances.
Roots Organic Gourmet is recalling Roasted Garlic Hummus because the label lists Tamari but lacks a 'Contains Soy' statement.