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.
INO Therapeutics is recalling 45 INOmax DSIR units because a specific software and display combination may trigger false alarms, interrupting nitric oxide therapy.
Urban Outfitters is recalling four styles of Cheeky Teacups because gold paint accents can spark in the microwave, posing a fire hazard.
Izzio Artisan Bakery is voluntarily recalling a specific lot of Lemon Poppy Muffins because the product is undercooked and may contain undercooked egg.
Kroger is recalling approximately 140,000 Kids Korner children's zipper hooded sweatshirts because the zipper pull can detach, posing a choking hazard to young children.
Blue Bird is recalling 2013-2016 All American and Vision school buses because incorrect fasteners may cause seat belts to be improperly anchored, increasing injury risk in crashes.
Mercedes-Benz is recalling certain CLS 400, 550, and 63 models because LED tail lights may not illuminate on the sides, reducing rear visibility and increasing crash risk.
K.J. Sportswear is recalling about 9,200 children's Thor pajamas because they fail to meet federal flammability standards, posing a risk of burn injury.
Comet USA is recalling about 2,100 efco gas trimmers because the engine muffler can break during use, posing a fire hazard. Consumers should stop using the units and return them for a free replacement.
Toyota is recalling 2012-2015 Yaris vehicles sold in Puerto Rico because the roof headliner may not provide proper occupant protection in a crash.
Winnebago is recalling 2015 ERA, View, and Itasca Navion vehicles because an incorrectly installed door component may make doors harder to open after a crash.
Harbor Freight is recalling specific Haul Master trailer light kits because they may fail to meet federal safety standards, potentially reducing trailer visibility to other drivers.
Rapala is recalling StrikeMaster Lithium Lazer ice augers because the trigger switch may fail to turn off the unit, posing an injury risk.
Forest River is recalling one 2015 XLR Hyperlite trailer because fuel vapors may ignite near a fuel-burning appliance. The unit is being repaired at the dealership before delivery.
PACCAR is recalling 2006-2016 Peterbilt trucks because tire labels may list incorrect pressure, risking tire failure and crashes.
Multiprens is recalling STK-100 triangle kits manufactured between October 2011 and July 2014 because they fail to meet Federal Motor Vehicle Safety Standard No. 125.
Navilyst Medical is recalling NAMIC Convenience Kits because expiration dating is not fully supported by shelf life testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 13 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 512 NAMIC Convenience Kits because expiration dating is not fully supported by testing, posing a potential sterility breach and infection risk.
Navilyst Medical is recalling 541 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 10 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.
Navilyst Medical is recalling 180 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, posing a risk of sterility breach and infection.
Taizhou Tianda is recalling 480 seat belts manufactured in 2013 because improper buckle manufacturing may prevent easy unlatching, potentially hindering vehicle egress during emergencies.
Zimmer GmbH is recalling 1,908 CoCr Femoral Heads due to potential sterile tray compromise. Undetected breaches could lead to contamination and periprosthetic infection.
Brainlab AG is recalling 114 Offset Cup Impactor Universal units because their sterilization parameters are ineffective. The recall covers units distributed worldwide prior to January 13, 2015.
Navilyst Medical is recalling 5 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.