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.
Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because an incorrect rear seat covering may hide the center child seat anchor point, increasing crash injury risk.
Mercedes-Benz is recalling 2018 CLA 250 and CLA 250 4MATIC vehicles because tail and side marker lights may flicker or fail, increasing crash risk.
Mercedes-Benz is recalling 2017-2018 C and E Class vehicles because front seatbacks may not lock properly, increasing injury risk in a crash.
JumpSport is recalling about 11,300 half-fold fitness mini-trampolines because the folding frame can forcefully hit users, causing cuts, bruises, and dental injuries.
Keystone RV is recalling certain 2018-2019 recreational trailers because cargo tray rivets may shear, allowing the tray to detach and potentially injure someone.
New England Wheels is recalling 2008, 2013, and 2014 Ford E-250 vans with Ricon wheelchair lifts because the positioning cam may fail, causing the platform to rise too high.
D&D Futon Furniture is recalling about 800 Sleeper Chair Folding Foam Beds because they fail to meet federal flammability standards, posing a fire hazard.
Foundation Ambulance is recalling 2017-2018 Type I and III ambulances because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.
Somerset Welding & Steel is recalling 2017-2018 J&J Truck Bodies Dump Bodies because brake lights may illuminate without the pedal being pressed, increasing crash risk.
Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter VS30 vehicles because the LED rear fog lights may fail to illuminate, increasing crash risk.
Volvo Bus is recalling 2015-2018 9700 motorcoaches because the fire extinguisher actuator may fail to discharge the suppression agent, increasing injury risk during a fire.
General Motors is recalling 2019 Cadillac CT6 vehicles because turn signals may not automatically cancel, potentially misleading other road users.
Winnebago is recalling 2014 Metro Link vehicles because a wheelchair lift cam may fail, causing the platform to rise too high and increasing injury risk.
SRAM is recalling i-Motion 3 internal gear hubs because the brakes can fail, posing crash and injury hazards to riders.
Shearwater is recalling yellow diving pressure transmitters because they may fail to signal tank pressure, posing a drowning hazard to divers.
Prevost is recalling 2015-2018 coaches and motorhomes because the fire extinguisher actuator may fail to discharge the suppression agent, increasing injury risk in a fire.
Porsche is recalling 2019 Cayenne and Cayenne S vehicles because a software failure may delay the rearview camera image display, increasing crash risk.
MORryde is recalling 1,541 recreational trailer chassis because cargo tray rivets may shear, causing the tray to detach and increasing crash risk.
Steris Corporation is recalling 129 ATLAS Loading Cars because the latch may fail to engage when empty, causing the unit to slide or fall.
Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Chip bars due to undeclared peanut. Consumers should stop eating the product.
Chicago Bar Company is voluntarily recalling RXBAR Mixed Berry bars due to undeclared peanut. Consumers should stop eating the product and return it to the store.
AtriCure is recalling 1,288 COBRA FUSION 50 Ablation Systems because patients may face an elevated risk of thromboembolism during specific off-pump procedures.
Promise Pharmacy is recalling 59 vials of IGF-1 LR3 injections because they lack sterility assurance. The affected products were distributed nationwide.
Philips is recalling 146 CombiDiagnost R90 X-ray systems because a software defect may cause patients to receive increased radiation doses.
Mylan Pharmaceuticals is recalling DrNatura Flora Protect Probiotics and Toxinout Kits due to an undeclared soy allergen statement.