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.
MiWorld Accessories is recalling iPhone 5/5S wall chargers sold at Charlotte Russe because they can overheat and catch fire. One fire incident was reported.
Kawasaki is recalling specific Vulcan 1700 Voyager and Vaquero motorcycles because an ignition wire may chafe against the fuel tank, causing a short circuit and potential engine stall.
Spartan Motors is recalling 2008-2010 Gladiator and MetroStar emergency vehicles because mirror lenses may fall off due to vibration, impairing driver visibility.
Micro Bird is recalling 2013-2015 G5 transit buses because corroded battery studs may cause short circuits and fires, or missing bolts may cause battery detachment.
Holley is recalling NOS-brand Nitrous Oxide systems manufactured between May and August 2015 because solenoid valves may fracture under pressure, posing an injury risk.
Huffy is recalling about 460 model year 2014 TR 745 and TR-S 740 bicycles because an open quick release lever can contact the front disc brake, causing a crash.
Tippmann Sports is recalling about 6,500 rental paintball markers because the trigger safety can fail, allowing paintballs to fire unexpectedly. No injuries have been reported.
Robert Bosch Tool is recalling Dremel MICRO Model 8050 rotary tools because the circuit board can overheat, melt the enclosure, and cause burns.
Freedom Snacks is recalling 50 bags of Sea Salt Caramel Gourmet Popcorn because milk is not declared on the label, posing a risk to consumers with milk allergies.
Trek is recalling about 330 Superfly bicycles because the carbon seatpost can crack and break, posing a fall hazard to the rider.
Winco Mfg. is recalling four Care Cliner X-Large chairs because the foam used was standard foam rather than fire-retardant foam.
California Qi Li's Braised Chicken is recalling approximately 6,644 pounds of duck head and neck products because they contain undeclared soy and wheat allergens.
Winco Mfg., LLC is recalling Care Cliner X-Large chairs because the foam was mislabeled as fire retardant but is actually standard foam.
Winco Mfg. is recalling XL Convalescent Recliners because the foam used was not fire retardant as required.
Winco Mfg., LLC is recalling Care Cliner Standart chairs because the foam used was not fire retardant as required.
Friendly Ice Cream Corp. is voluntarily recalling 20,736 tubs of Vienna Mocha Chunk Ice Cream due to the potential presence of a foreign object.
American Science & Engineering is recalling 125 Gemini Cabinet X-ray systems because a fault may cause X-rays to be produced without the indicator lights illuminating.
Winco Mfg. is recalling 32 Elite Care chairs because foam shipped as fire retardant was actually standard foam, failing safety standards.
Teleflex is recalling Bronchial One Lumen Tubes because the cobb connector may detach from the main connector prior to use.
Winco Mfg. is recalling three Drop Arm Care Cliner chairs because the foam used was not fire retardant as required.
Winco Mfg., LLC is recalling two Designer Care Cliner chairs because the foam used was not fire retardant as required.
Winco Mfg. is recalling specific patient recliners because the foam used was standard foam rather than fire-retardant foam, failing to meet safety standards.
Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.
Siemens Medical Solutions is recalling Symbia T Series imaging systems because improper fuses could cause the Power Controller assembly to overheat.
Teleflex is recalling Bronchial One Lumen Tubes - Left because customer complaints reported the cobb connector detaching from the main connector prior to use.