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.
Angiotech is recalling specific lots of bone marrow biopsy needles because a manufacturing issue may have compromised the sterile seal on the blister trays.
GE Healthcare is recalling 131 Revolution CT systems with the SmartStep Option because the displayed Z location may not match the actual table position, potentially causing scans at incorrect locations.
Handpiece Headquarters is recalling 252 Henry Schein CU 1000 Halogen Curing Lights because the tip became too hot, causing heat sensations in patients.
Shop LC is recalling rechargeable disco ball LED lights because the batteries can overheat while charging, posing burn and fire risks.
Mrs Grissom's Salads, Inc. is recalling 407 cases of Pimento Cheese and Cranberry Pecan Chicken Salad due to an undeclared milk allergen.
Angiotech is recalling 500 units of Double Diamond J Type Bone Marrow Needles due to a manufacturing defect in the sterile seal on blister trays.
Angiotech is recalling 180 units of J Type Bone Marrow Needles due to a manufacturing issue affecting the sterile seal on blister trays.
GE Healthcare is recalling Centricity Universal Viewer Breast Imaging software because a display error could lead to incorrect patient diagnoses.
Stryker is recalling Naera Hospital Bassinet mattresses because air expansion at high altitudes may create gaps, posing a risk of patients rolling over.
Target is recalling Cat & Jack toddler boots because the unicorn horn can detach, posing a choking hazard to children.
ASA Electronics is recalling Voyager monitors that may revert to factory settings, causing the backup camera image to reverse and increasing crash risk.
Blue Bird is recalling one 2019 Vision bus because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.
Lakota is recalling 2018-2019 Bighorn, Charger, Colt, and Livestock Edition trailers because incorrect tire data on the Federal Placard could lead to tire overload and failure.
Forest River is recalling 2019 Wildwood recreational trailers because the Federal Placard lists an incorrect front tire pressure of 110 PSI instead of 80 PSI.
Ford is recalling 2019 Mustang, Lincoln Nautilus, and Navigator vehicles because the instrument cluster may display blank, hiding critical safety information.
Blue Bird is recalling 2015-2019 Vision and All American school buses because a wheelchair lift component may fail, causing the platform to rise too high and increasing the risk of injury.
Hickory Springs is recalling FB11-39 DRW restraining barriers because they may fail to restrain unbelted occupants during a crash, increasing injury risk.
Forest River is recalling 2019 Cherokee recreational trailers because the Federal Placards list incorrect tire size information, which may lead to the installation of insufficient tires.
Isuzu is recalling 2019 NPR and Chevrolet 4500/5500 trucks because the odometer may display kilometers instead of miles, potentially delaying critical maintenance.
Forest River is recalling 2018-2019 Rockwood and Flagstaff recreational trailers because bunk bed door latches may fail, allowing the door to open while moving.
General Motors is recalling specific 2016-2018 Cadillac and Chevrolet vehicles because the electric power steering system may fail, increasing crash risk.
Grand Strand Sandwich Company is recalling 420 cases of Ham & Cheese Lunch Box Sandwiches due to potential Listeria monocytogenes contamination.
Roche Diagnostics is recalling Anti-HAV IgM test systems due to potential erroneous result messages on the cobas e 602 module.
Medtronic is recalling 1,100 Reservoir Y Adapters because the Y-connectors may tear or crack, potentially causing blood loss and circuit breaches during autotransfusion.
Grand Strand Sandwich Company is recalling 140 cases of Ham & Cheese Croissant Lunch Box Sandwiches due to potential Listeria monocytogenes contamination. The product was distributed in North Carolina and South Carolina.