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.
Dressen is recalling 2006-2013 Dakota Cargo and Competitor trailers because a door lock defect could jam the deadbolt, trapping occupants inside.
Toys R Us is recalling Journey Girl Travel Trunks because the blue metal handle can be sharp and cause lacerations. Consumers should stop using the trunks and return them for a refund.
Nissan is recalling 2006-2010 Infiniti M35 and M45 vehicles because the accelerator pedal sensor may fail, causing the engine to stall and increasing crash risk.
Prevost is recalling specific model year 2005-2014 buses because the certification plate lists incorrect tire inflation pressures, which may lead to overinflation and increased crash risk.
Eagan Manufacturing is recalling 2006-2013 trailer doors with Fastec locks that may jam, potentially trapping occupants inside.
Nissan is recalling 2,310 2014 Pathfinders because a manufacturing error may prevent the passenger air bag from deploying properly in a crash.
American Hauler is recalling 2006-2010 cargo trailers equipped with a specific door lock option that may jam, potentially trapping occupants inside.
Toyota is recalling 2004-2005 and 2007-2009 Sienna minivans because the shift lever may move out of Park without the brake pedal being depressed, increasing crash risk.
Volvo Bus is recalling 2013 9700 coach buses because a manufacturing error may cause the parking brake to fail to fully apply, increasing crash risk.
Smith & Nephew is recalling OSTEORAPTOR 2.3 mm Suture Anchors because pinholes in primary pouches may breach the sterile barrier.
Smith & Nephew is recalling OSTEORAPTOR 2.9 mm Suture Anchors because pinholes in primary pouches may breach the sterile barrier.
GE Healthcare is recalling READY View software because it may compute and display incorrect fMRI activation maps.
Medtronic is recalling nine T8 Removal Heads used in spinal surgery due to incorrect hardness specifications that could cause the tool to fail during implant removal.
GE Healthcare is recalling CARESCAPE Monitor B650 units due to potential issues. No injuries or illnesses have been reported.
Smith & Nephew is recalling OSTOSTEORAPTOR 2.9 mm Suture Anchors because pinholes in primary pouches may breach the sterile barrier.
Instrumentation Laboratory is recalling 929 ACL TOP analyzers because a potential carryover issue may cause shortened APTT clotting times.
Churchill Medical Systems is recalling 13,100 Vygon 14 Microbore Extension Sets because the tubing may disconnect from the male luers.
Villa Radiology Systems LLC is recalling 22 Juno DRF mobile X-ray systems because displayed radiation dose values may be inaccurate by more than 35%.
Smith & Nephew is recalling TWINFIX ULTRA suture anchors because pinholes in primary pouches may breach the sterile barrier.
Lucy's Kitchen, Inc. is recalling Superpan Tu Pan Natural because the ingredient list declares 'semolina durum' but omits the common name 'wheat', an undeclared allergen.
Mike's Quality Meats, Inc. is recalling frozen hot smoked salmon due to missing storage instructions on the label, which could allow Clostridium botulinum to grow.
Smith & Nephew is recalling OSTEORAPTOR suture anchors because pinholes in primary pouches may breach the sterile barrier. The recall covers 10,296 units distributed worldwide.
Instrumentation Laboratory is recalling ACL TOP 500 CTS analyzers due to a potential carryover issue that may cause shortened APTT clotting times.
Instrumentation Laboratory is recalling 662 ACL TOP 300 and ACL TOP 300 CTS analyzers worldwide due to a potential carryover issue that may cause shortened APTT clotting times.
Lucy's Kitchen, Inc. is recalling 150 units of Superbudin because it contains undeclared wheat and soy. The product was distributed only in Puerto Rico.