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.
Trane and American Standard are recalling specific accessory heaters installed in air handlers due to a fire hazard caused by overheating.
General Motors is recalling specific 2005-2009 models because the headlamp driver module may overheat and fail, causing lights to stop working.
American SportWorks is recalling about 3,500 four-wheel off-road utility vehicles because the throttle may fail to return to idle, posing a risk of injury.
J.M. Mattress is recalling about 240 renovated mattresses that fail federal flammability standards, posing a fire hazard.
Southeast Toyota Distributors is recalling 2010-2015 Toyota 4Runners because accessory exhaust tips may contact people and cause burns.
Halcore Group is recalling 2014-2015 AEV Trauma Hawk emergency vehicles because the backup camera may display reversed images, increasing crash risk.
Toyota is recalling 949 model year 2015 Prius C vehicles because the tire pressure monitoring system may fail to warn drivers of low tire pressure, increasing crash risk.
Siemens is recalling one Biograph mCT S(40)-4R unit because it may be missing a locking ring on the optional ceiling mount.
Midlon Foods Inc. is recalling 5,472 units of Maria Biscuits because misaligned labels covered the allergen warning statement.
Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assemblies because the locking collars are not locking.
Siemens Medical Solutions is recalling specific CT systems because optional ceiling mounts may be missing a locking ring.
The Apothecary Shoppe LLC is recalling SIU-Prostaglandin E1 500 mcg/mL Injection vials in Oklahoma due to lack of documentation for environmental monitoring during production.
Siemens Medical Solutions is recalling Axiom Artis angiography systems because liquid may seep through the top cover and penetrate internal components, potentially disabling table movements.
Pierce is recalling 2014-2015 Velocity and Quantum vehicles because LED headlamps may flicker in extreme cold, reducing visibility and increasing crash risk.
Flowers By Zoe is recalling girls' striped hoodies and tie-dye jackets because neck drawstrings pose a strangulation hazard to children.
Siemens is recalling ACUSON S Family ultrasound systems because biopsy needles may move outside the on-screen guidelines when using specific attachments.
Siemens Medical Solutions is recalling Artis zee angiography systems because liquid may seep through the table cover, potentially preventing table movement.
The Apothecary Shoppe is recalling specific lots of Testosterone Cypionate Injection due to a lack of documentation confirming proper environmental monitoring during production.
Nissan is recalling 2012-2015 Versa and 2014-2015 Versa Note vehicles because a center console trim panel may catch the driver's shoe, delaying brake application and increasing crash risk.
Paleteria La Jalpita is recalling Coco (Coconut) Popsicles due to undeclared sulfite. The product was distributed in Oregon and Washington.
The Apothecary Shoppe LLC is recalling SIU-Prostaglandin E1 20 mcg/mL Injection due to a lack of documentation ensuring proper environmental monitoring during production.
Teva Pharmaceuticals is recalling specific lots of amphetamine tablets because they failed impurity specifications. The product contains an unknown impurity.
The Anspach Effort, Inc. is recalling Synthes Battery Power Line II Oscillator Model 530.710 units because the saw head may separate from the drive unit or come loose.
Merge Healthcare is recalling 451 Merge Hemo systems used with Masimo PHASEIN modules due to system freeze-ups that required moving patients to other cath labs.
Chrysler is recalling 2014 Jeep Cherokee vehicles because using front wipers on dry glass may damage the body control module, potentially causing wiper failure and impaired vision.