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.
Jayco is recalling 2019 Precept and Precept Prestige motorhomes because improperly heat-treated front wheel studs may break, increasing crash risk.
AAA Innovations is recalling about 275 promotional cooler grills because the wooden cabinet can catch fire. No injuries have been reported.
Entegra is recalling 2019 Anthem, Aspire, Cornerstone, and Insignia motorhomes because improperly adjusted entry door latch rods may allow the door to open during transit.
Jayco is recalling 2019 Jay Flight travel trailers because incorrectly wired turn signal and brake lights may fail to operate, increasing crash risk.
Mercedes-Benz is recalling certain 2016-2018 GLC models because rear seat belt latch plates may retract into the interior paneling, preventing use.
UberScientific is recalling Uber Numb topical anesthetic cream and spray because the packaging is not child-resistant, posing a risk of poisoning to young children.
Boy Story is recalling Mason and Billy action dolls because the vinyl joints can break, creating pieces that pose a choking hazard to young children.
Integrated Tower Systems is recalling 2007-2018 Mobile Tower trailers because a missing power disconnect on the control panel may cause electrical shock.
Honda is recalling 2019 Insight, Odyssey, and Ridgeline vehicles because a manufacturing error in the SRS control unit may prevent air bags or seatbelt pretensioners from deploying in a crash.
Honda is recalling 2017-2018 Civic and CR-V vehicles because a loose magnet in the electric power steering system may cause unintended steering input, increasing crash risk.
TerraTrike is recalling 600 adult tricycles because the right wheel hub mount can bend or break, creating a crash risk.
IKEA is recalling CALYPSO ceiling lamps because the glass shade can detach and fall, posing impact and laceration hazards. Consumers should stop using the lamps and return them for a refund or replacement.
Degania Silicone is recalling 153 temperature sensor Foley catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Coviden is recalling temperature sensing Foley catheters that may display lower body temperature measurements than the patient's actual temperature.
Spartan Motors USA is recalling 2019 Spartan K2 Specialty vehicles because upper mounting fasteners may puncture the air spring bag, increasing crash risk.
Degania Silicone is recalling 89,122 Foley catheters with temperature sensors because defective sensors may display lower body temperatures than the patient's actual temperature.
ShinChang Medical Co., Ltd. is recalling 6,570,800 disposable insulin syringes because a small crack was found in the top end of the barrel near the needle.
EOS Imaging is recalling 17 sterEOS workstations because 3D projections may be incorrect when using specific secondary image captures, potentially leading to clinical errors.
Degania Silicone is recalling 4,332 Foley catheters with temperature sensors because defective sensors may display lower body temperatures than the patient's actual temperature.
bioMerieux is recalling VITEK 2 AST-P655 cards because six lots were manufactured with insufficient gentamicin, potentially affecting high-level resistance screening results.
Degania Silicone is recalling 330 Thermistor Foley catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Degania Silicone is recalling 500 units of temperature sensor Foley catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Fresenius Medical Care is recalling 40 units of the 2008T Hemodialysis System because a power failure during cleaning could leave disinfectant in the dialysate delivered to patients.
Permobil is recalling 3,134 powered wheelchairs because backrest support bars may fail, potentially causing users to fall backward and sustain injuries.
Degania Silicone is recalling 250 Foley Temperature Sensor Catheters because defective sensors may display lower body temperatures than actual.