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.
Aston Martin is recalling specific 2010-2016 models because interior door unlocking mechanisms may fail when locked from outside, potentially trapping occupants.
Sterilmed is voluntarily recalling reprocessed tourniquet cuffs because the company cannot assure the sterility of all units in the affected lots.
First Source LLC is recalling Wegmans Dark Chocolate Pistachio Toffee because it contains undeclared cream (milk). The product was sold in New York.
GE Medical Systems is recalling 125 Revolution CT scanners worldwide due to potential image artifacts in head scans that may mimic pathology. No injuries have been reported.
LeMaitre Vascular is recalling 4,315 Over-the-Wire Embolectomy Catheters due to a manufacturing issue that could compromise sterility.
Skipanon Brand Seafoods LLC is recalling all cans and pouches of its seafood products due to lack of documentation and possible under-processing, which could lead to Clostridium botulinum contamination.
Lakeside Foods is recalling 16 oz bags of French Style Green Beans due to potential Listeria monocytogenes contamination.
Philips is recalling Brilliance CT scanners with software version 2.0 because a printing error may display incorrect tumor locations, potentially leading to patient mistreatment.
Skipanon Brand Seafoods is recalling canned smoked peppered Chinook salmon due to lack of documentation and possible under-processing, which could allow Clostridium botulinum contamination.
Visicu, Inc. is recalling 43 units of eCareManager software due to a defect that may cause incorrect medication orders to be displayed and signed.
LeMaitre Vascular is recalling 4,315 embolectomy catheters worldwide due to a manufacturing defect that may compromise packaging sterility.
Norpac Foods is recalling IQF Cut Wax Beans due to Listeria monocytogenes contamination. The product was distributed to food service accounts in seven states.
Olympus is recalling 182 ENDOEYE HD II video telescopes because a damaged temperature sensor can cause the tip to overheat, posing a burn risk to patients and users.
Lithonia Lighting is recalling JHBL LED fixtures because the mounting hub can break, causing the fixture to fall. No injuries have been reported.
Open Range is recalling 2014-2015 3X recreational trailers because a missing caution label may allow sewer gas to escape if the drain valve is left open.
McLaren is recalling 122 model year 2014-2015 P1 hybrid vehicles because the secondary hood latch may fail to re-engage, potentially allowing the hood to open while driving.
General Motors is recalling 2,633 model year 2016 Chevrolet Traverse, GMC Acadia, and Buick Enclave vehicles because the third-row left lower seat frame may have welds in incorrect locations.
Highland Ridge RV is recalling specific 2015-2016 fifth wheels and travel trailers because they may be missing a caution label regarding the sewer drain valve.
Trail Boss is recalling one 2013 Bloomer Horse Trailer because a water heater valve may cause overheating, posing a scalding risk.
Forest River is recalling 2016 model year recreational trailers that were not equipped with carbon monoxide detectors, increasing the risk of injury to occupants.
Dollar Tree is recalling Assured Burn Relief Gel because the packaging is not child-resistant, posing a poisoning risk if swallowed.
Cooper Tire & Rubber Co. is recalling specific Zeon LTZ tires manufactured in September 2015 because tread cracking or chunking may cause loss of tire pressure, increasing crash risk.
Halcore Group is recalling 18 model year 2015 Horton ambulances because an incorrectly installed circuit board component may cause electrical system failure, potentially disabling life-saving equipment.
DeRoyal Industries is recalling four lots of Hydro-Temp Neonatal Temperature Skin Sensors because incorrect soldering prevents temperature readings on infant warming systems.
Life Science Pharmacy Inc. is recalling compounded Estriol Suppositories because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.