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.
Turtle Top is recalling certain 2007-2012 Ford Odyssey, Terra Transport, and Van Terra vehicles equipped with Ricon wheelchair lifts. An armored cable may not clear the lift, potentially causing a short circuit and fire.
Zero Motorcycles is recalling 2013 FX and XU motorcycles because a battery sealant defect may allow water penetration, potentially causing burns.
Collins Bus is recalling 17 model year 2006-2007 Mid Bus CSD-7450R-C vehicles because a wheelchair lift cable may cause a short circuit and fire.
Kichler Lighting is recalling Aztec chandeliers sold at Lowe's because the fixture loop can fail, causing the light to fall from the ceiling.
Purely American, Inc. is recalling specific 10 oz bags of Pasta Salad Mix because the labels are missing the required wheat allergen declaration.
OrthoPediatrics Corp is recalling 130 90 Degree Cannulated Infant Blade Plates due to reports of the plates bending during surgery.
OrthoPediatrics Corp is recalling 90 Degree Cannulated Infant Blade Plates due to reports of the plates bending during surgery.
Purely American, Inc. is recalling Chicken Noodle Soup Mix because some labels are missing the required wheat allergen declaration.
Bard Peripheral Vascular is recalling 815 UltraClip breast tissue markers because they were distributed without completing the sterilization process.
OrthoPediatrics Corp is recalling 90 Degree Cannulated Infant Blade Plates due to reports of the plates bending during surgery.
Purely American, Inc. is recalling 73 bags of Gilroy Garlic Pasta Stir Fry Mix because the labels are missing the required wheat allergen declaration.
Whole Foods Market is recalling Natures Path Hemp Plus Granola sold in bulk bins because it may contain undeclared almond slices.
Bard Peripheral Vascular is recalling 223 Usher Support Catheters that were distributed without completing the sterilization process.
Purely American, Inc. is recalling Shenandoah Valley Apple and Spice Cake Mix because some labels are missing the required wheat allergen declaration.
Purely American, Inc. is recalling Santa Fe Cornbread Mix because the labels are missing the required wheat allergen declaration.
Bard Peripheral Vascular is recalling 17 MicroSheath and Usher support catheters because they were distributed without completing the sterilization process.
Edwards Lifesciences is recalling QuickDraw Venous Cannulas because the device may separate during withdrawal when using the percutaneous insertion method.
Purely American, Inc. is recalling Adirondack Getaway Pasta Toss Mix because some labels are missing the required wheat allergen declaration.
Easton is recalling specific batches of Axis archery arrows because they can break when fired, posing a risk of injury to users and bystanders.
Purely American, Inc. is recalling specific varieties of Pasta Salad Mix because the labels are missing the required wheat allergen declaration.
Purely American, Inc. is recalling Indian River Orange Drop Cookies Mix because the labels are missing the required wheat allergen declaration.
American Importing Co, Inc is recalling Market Pantry Sweet & Salty Mix because it contains Butter Toffee Peanuts with undeclared milk.
Applied Medical is recalling specific lots of Epix and Direct Drive Laparoscopic Graspers because the trigger may fracture, potentially leaving the jaws closed.
Abbott Medical Optics is recalling STAR S4 Excimer Laser Systems due to an unlikely potential for inadvertent laser firing under specific conditions.
Abbott Medical Optics is recalling 1,882 STAR S4 IR Excimer Laser Systems worldwide due to an unlikely potential for inadvertent laser firing under specific conditions.