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.
Honda is recalling certain 2020-2021 Insight, 2020 CR-V Hybrid, and 2020 Accord Hybrid vehicles due to a DC-DC converter fault that may prevent battery recharging, potentially causing loss of drive power and increasing crash risk. Owners can receive a free software update.
Land Rover is recalling 2020 Range Rover Evoque vehicles because the front seat material may burn too quickly in a fire, increasing injury risk.
Ford is recalling certain 2021 E-350 and E-450 vehicles due to mispositioned engine cover insulation that may cause excessive heat and burns to occupants.
USDA FSIS issued a public health alert for Country Meats HOT BBQ Flavor Smoked Pork Snack Sticks due to misbranding and an undeclared milk allergen.
General Motors is recalling 2021 Cadillac Escalade vehicles because the front passenger seat belt and airbag status lights may be invisible in daytime, increasing crash injury risk.
JMH International is recalling Chef Myron's Premium Teriyaki Sauce because it contains wheat-derived gluten despite a gluten-free claim.
Clinical Innovations is recalling ROM Plus Collection Kits because incorrect swabs may cause false test results.
Camp Chef is recalling about 20,600 portable gas stoves because a sharp edge on an internal gas regulator part can cause gas leaks, posing a fire hazard.
Medtronic is recalling 71,030 Evolut PRO System units worldwide due to a potential for transcatheter aortic valve leaflet damage during post-implant balloon dilatation.
Mani, Inc. is recalling Trocar Kit 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or disconnection during ophthalmic surgery.
Kroger is recalling HomeChef Pretzel-Crusted Chicken meal kits because a supplier ingredient was suspect for Listeria species.
Graco is recalling inclined sleeper accessories for four playard models due to a risk of infant suffocation. Consumers should stop using the accessory immediately and contact Graco for a refund.
Avanos Medical is recalling 710 units of CORFLO NG/NI Pediatric Neonatal Feeding Tubes because the male AIV adaptor may detach from the Y-connector.
Pacific Coast Producers is recalling Italian Style Tomato Paste in 6 oz. cans due to the presence of metal shavings. The product was distributed under several grocery store brands.
Philips is recalling 16 IntelliVue X2 Multi Measurement Servers because speaker failures may prevent audible alarms, potentially delaying patient treatment.
Shimadzu Medical Systems is recalling 22 MH-200S X-Ray systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.
Medtronic is recalling Evolut R System transcatheter aortic valves due to a potential risk of leaflet damage during post-implant balloon dilatation.
K2M, Inc. is recalling 197 units of the Everest MI XT Tab Removal Tool because the threaded interface may crack, causing Loctite to leak from the handle.
JMH International is recalling Chef Myron's Szechuan Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.
Medtronic is recalling 19,961 Evolut PRO+ Transcatheter Aortic Valve systems due to a potential for leaflet damage during post-implant balloon dilatation.
Chromsystems Instruments & Chemicals GmbH is voluntarily recalling 342 vials of MassChrom Amino Acid Analysis Plasma Control Level III due to a Class II device defect.
Cycling Sports Group is recalling about 1,270 Cannondale Canvas NEO e-bicycles because the front fender can detach and stop the wheel, posing a fall hazard.
Mani, Inc. is recalling MANI Infusion Cannula 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or unintended disconnection during ophthalmic surgery.
TissueTech, Inc. is recalling 10 units of PROKERA Plus non-sterile biologic corneal bandages due to potential exposure to microbial contamination.
Riverside Natural Foods is recalling Good & Gather Banana Chocolate Chip Date & Nut Bars because they contain undeclared almonds.