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.
Spartan Fire is recalling 2024-2025 fire trucks because a missing mechanical stop may allow the cab tilt cylinder to overextend, potentially causing the cab to drop.
Nissan is recalling certain 2023-2024 Z vehicles because right-side pedestrian detection sensor connectors may be reversed, preventing the pop-up engine hood from activating.
Chrysler is recalling certain 2020-2023 Pacifica and Voyager vehicles because an improperly secured side curtain airbag connector may prevent the airbags from deploying.
CFMOTO is recalling about 2,650 of its 2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring ATVs because the throttle lever can fail to return to idle, causing unexpected acceleration and crash risk. One minor injury has been reported.
Orange EV is recalling 2017-2024 T-Series and 2023-2024 e-TRIEVER trucks because manuals incorrectly describe the high-voltage lockout procedure, posing an electrical shock risk.
GM is recalling certain 2025 Cadillac XT4 vehicles because the instrument panel may be missing the perforation that allows the passenger-side airbag to deploy properly.
Chrysler is recalling 2025 Ram 1500 vehicles because damaged front wheel hub encoder rings can disable the electronic stability control system, increasing crash risk.
PowerBlock is recalling about 1,845 Commercial Pro 100 weight sets sold with 5 lb grip handles because weight plates above 55 lbs can dislodge during use, posing an impact injury risk.
Newmar is recalling 2023-2025 Super Star motorhomes because damaged inner tire valve extensions can cause tire failure and increase crash risk.
Silver Eagle is recalling specific eye and shank assemblies because welds may crack, allowing the eye to separate from the trailer converter dolly and increasing crash risk.
Volvo is recalling 2020 hybrid models because a loose brake pedal screw may cause loss of braking function, increasing crash risk.
Nuts.com is recalling S'mores Bites due to undeclared milk allergen. Milk chocolate was listed in the product description but omitted from the ingredient list, creating a labeling mismatch.
Bionpharma Inc. is recalling Atovaquone Oral Suspension (750 mg/5 mL) nationwide due to Cohnella bacteria contamination. The recall affects 1,980 bottles.
Nova Ortho-Med is recalling 1,886 MONARCH ROLLATOR BLUE rolling walkers due to a potential fall hazard. The backrest may disengage when users shift from a slouched to upright seated position.
Leica Biosystems is recalling the Cryostat Model CM1900 because its labeling lacks a warning about using flammable freezing sprays in the chamber. The sprays can ignite, creating a serious fire and burn hazard.
Merit Medical Systems is recalling basixTOUCH Inflation Devices due to a potential hole in the sterile barrier. The defect may expose patients to pathogens and pyrogens, increasing infection risk.
Merit Medical Systems is recalling 429 IntelliSystem Inflation Devices due to a potential hole in the sterile barrier that could allow pathogen exposure and infection.
Boston Scientific is recalling AVVIGO+ Multi-Modality Guidance Systems due to a software error that displays incorrect 9-grid marks instead of 15-grid marks in Live and Record modes. This display error could affect physicians' ability to set proper reference depths during intravascular imaging procedures.
Medline Industries recalls certain open-heart surgical kits (Lot 23LBR364) due to incorrect model labeling, where model 30001 units were labeled as model 30000. The recall affects 30 units distributed nationwide.
Merit Medical Systems is recalling 202 StabiliT TOUCH Syringes with potential small holes in the sterile barrier. Affected devices may expose users to pathogens and pyrogens, which could cause infection.
Leica Biosystems recalls its Cryostat Model CM1100 due to inadequate warnings about using flammable freezing sprays, which can ignite and cause serious injuries. The device labeling lacked required safety warnings prior to 2019.
Horizon Cardiology Hemo Version 12.2 is recalled for a unit-of-measurement configuration issue that can produce incorrect hemodynamic calculations, potentially resulting in misdiagnosis and inappropriate treatment. The recall affects 3 worldwide systems.
Gorilla Mind Rauwolscine dietary supplement is recalled nationwide due to potential Salmonella contamination. Consumers should not use the product and contact the manufacturer.
Boston Scientific is recalling the AVVIGO+ Guidance System due to a software bug displaying incorrect grid marks during live imaging. The device shows 9 grid marks instead of 15, which could affect accurate vessel measurement in cardiac interventions.
Boston Scientific is recalling the AVVIGO+ Multi-Modality Guidance System due to a software error that displays an incorrect 9-grid overlay instead of the correct 15-grid overlay in Live or Record mode, affecting measurement accuracy with OptiCross 18 catheters.