State
73,100 recalls have nationwide distribution and so reach Kentucky. 7,194 additional recalls listed Kentucky specifically in their distribution scope.
Of the 7,194 recalls naming Kentucky we have scored against our rubric, 1,409 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,706 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,194 recalls whose distribution notice names Kentucky specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
COCA COLA Consolidated LLC recalls Minute Maid Zero Sugar Lemonade cartons sold in Indiana, Kentucky, and Ohio. Regular Minute Maid Lemonade cans were incorrectly placed in Zero Sugar packaging.
Enterprise Imaging XERO Viewer incorrectly displays reference lines on medical images due to a software defect affecting images with non-square pixel spacing. The misplaced reference lines may lead to diagnostic errors.
The FDA is recalling the Triathlon Universal TS Baseplate Size 2 knee implant due to defective locking tabs that may not properly engage with the tibial insert, potentially causing implant failure.
Medline is recalling approximately 9,608 automatic digital blood pressure units due to a faulty microchip that causes power failures, display issues, and overheating.
Integra LifeSciences recalls MEDIHONEY Dressing applicator pouches due to potential pinholes that may compromise sterility. The recall affects approximately 120,124 units distributed across 36 US states and internationally.
Windstone Medical Packaging is recalling Aligned Medical Tonsil Pack kits due to a component under recall for improper use. Approximately 180 packs were distributed nationwide.
Windstone Medical is recalling 894 Aligned Medical Tonsil ENT Packs containing Cardinal Health Salem Sump PVC tubes due to improper use concerns with a component under a separate recall action.
Howmedica Osteonics Corp. is recalling 897 MAKO Integrated Cutting System (MICS) Handpieces worldwide due to a manufacturing characterization process error that resulted in incorrect constant values being assigned to affected units.
Atrium Medical Corporation is recalling 11 iCast Covered Stents (Model 42616) due to an error in the Unique Device Identifier (UDI) printed on the distribution label. No illnesses or injuries have been reported.
FDA recall of 152 Inspire Model 4340 Respiratory Sensing Lead units due to a labeling error—the serial number printed on the product box does not match the actual serial number of the device inside.
Windstone Medical Packaging is recalling Aligned Medical T and A Pack REF AMS11482 because it contains a component subject to a separate recall action for improper use.
Inspire Medical Systems is recalling 457 Model 4063 Stimulation Leads because the serial number on the shelf box does not match the serial number of the device inside, creating identification and traceability issues.
The Aligned Medical Septo Pack (AMS11480) is recalled because it contains a Cardinal Health Salem Sump PVC tube component that is subject to an FDA recall for improper use.
BMW is recalling 2018–2022 X3 vehicles because rear cargo rail attachment bolts may become damaged in a rear crash, causing the rail to detach and increasing injury risk. Dealers will replace the bolts free of charge.
Certain 2024 Toyota Sequoia Hybrid, Tundra, and Tundra Hybrid vehicles are recalled due to passenger-side front and rear tire sidewall damage that may cause sudden tire pressure loss and loss of vehicle control.
Lamborghini is recalling 2024 Revuelto vehicles because a wiper connecting rod may bend and separate, causing wiper failure and reduced visibility.
McNeilus is recalling 2010-2024 Rear Loader vehicles because the license plate light is installed in the wrong location, potentially failing to fully illuminate the plate.
Honda is recalling certain 2023-2025 model year Civic vehicles because the high-pressure fuel pump may crack and leak fuel, increasing the risk of fire if an ignition source is present. Owners should contact Honda for free inspection and replacement.
Orscheln is recalling specific Electronic Throttle Pedal Assemblies because an oversized magnet carrier may cause the pedal to stick, increasing crash risk.
Jayco is recalling 2,044 units of 2021–2025 Entegra Ethos and Jayco Swift vehicles due to an incorrect Tire and Loading Information Label. The mislabeled tire load range could lead owners to select underrated replacement tires, increasing crash risk.
Bendix is recalling EC80 Electronic Control Units where electrical noise may cause safety systems to fail, increasing crash risk.
Hyundai is recalling 2019-2024 Nexo vehicles because the hydrogen pressure relief device may fail and leak, creating a fire risk. Owners are advised to park outside until the repair is complete.
Blue Bird is recalling 2020-2024 All American and 2021-2024 Vision transit buses because emergency exit labels are too small to read, potentially delaying evacuation.
Blue Bird is recalling 2019-2024 Vision and All American school buses because emergency exit labels are too small to read, potentially delaying evacuation.
E-One is recalling 282 fire trucks because a broken engine crossmember can damage the cooling fan, causing an engine stall and increasing crash risk.