State
73,187 recalls have nationwide distribution and so reach Kentucky. 7,195 additional recalls listed Kentucky specifically in their distribution scope.
Of the 7,195 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 1,707 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,195 recalls whose distribution notice names Kentucky specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling certain 2020-2024 Lincoln Aviator vehicles because electromagnetic interference from a cell phone can cause the rearview camera image to flicker or distort.
Mercedes-Benz is recalling 2023 AMG C43 vehicles because incorrectly routed seat wiring may damage the harness, preventing seat air bags from deploying in a crash.
KME is recalling 2022-2023 Predator fire trucks because an incorrect relay valve may prevent the parking brake from engaging, allowing the vehicle to roll away.
Blue Bird is recalling 2021-2023 Vision school buses because the diesel tank for the fuel-fired heater may leak fuel, creating fire and crash risks.
Altec is recalling certain 2020-2024 LR7 and LR8 aerial devices because a hydraulic cylinder feeder tube may become damaged and leak oil, which can result in uncontrolled boom movement.
Land Rover is recalling certain 2018-2022 Range Rover Sport vehicles with a Surround Camera System because water may enter the rearview camera, blanking or distorting the image.
GM is recalling certain 2024 Chevrolet Colorado vehicles because incorrect tires may have been installed that do not match the tire label, and the TPMS may report inaccurately.
Nexxpro is recalling NEXX X.G10 helmets in sizes M and S because they may lack a required carbon layer, failing to provide adequate protection in a crash.
Rivian is recalling certain 2023-2024 EDV, R1S and R1T vehicles because the headlights may be improperly aimed, failing FMVSS 108. 2,334 units are affected.
TOPINCN pool drain covers do not meet safety standards under the Virginia Graeme Baker Pool and Spa Safety Act, creating a risk of entrapment to swimmers and bathers. About 340 units sold online through Amazon from September 2022 through March 2024 are affected.
Diamond Coach is recalling 2023-2024 VIP 2200 transit buses because the seat recliner mechanism may not engage, increasing injury risk during a crash.
Apollo Tires is recalling specific Vredestein tires because a contaminated compound may cause steel belts to separate, increasing the risk of a crash.
QUIDELORTHO's VITROS Free T3 Reagent Packs may produce falsely elevated test results, potentially affecting thyroid function diagnoses and patient management. Eight lot numbers with expiry dates through August 2024 were distributed worldwide.
Sophysa is recalling the Pressio Ventricular Intracranial Pressure Monitoring Kit due to a manufacturing defect that causes cerebrospinal fluid leakage. An undetected leak during implantation could pose an infectious risk to patients.
M-C McLANE INTERNATIONAL is recalling canned jalapenos due to potential glass contamination. The voluntary recall affects 2991 cases distributed across 27 states.
Philips Patient Information Center iX software version 4.x fails to properly save or transfer event catalog information, risking data loss in healthcare facilities. The FDA issued a Class II recall affecting 358 units globally.
Ossur H/F is recalling RHEO KNEE prosthetic knee components due to firmware issues that could cause unintended warnings and device shutdown, creating fall risk for users.
Medline Industries recalls multiple namic CONVENIENCE KIT variants used in cardiovascular procedures due to lack of sterility assurance. Approximately 570 units distributed nationwide may pose infection risk.
Philips Ingenia 3.0T MR systems with software R5.7.1 may fail to warn about low ventilation, potentially causing patient overheating or burning sensations. 19 units affected worldwide.
Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension due to foreign material found in reconstituted bottles. This FDA Class II recall affects 17,040 bottles distributed nationwide.
Lupin Pharmaceuticals is recalling Cefdinir Oral Suspension USP 250 mg/5 mL (Lot F305442, expiration 8/30/2025) due to foreign material found in reconstituted bottles. Approximately 17,070 bottles were distributed nationwide.
QUIDELORTHO is recalling VITROS Free T3 Calibrators used in thyroid testing because they may produce elevated results that could lead to incorrect patient diagnosis or delayed care.
LeMaitre Vascular is recalling 5,604 units of Syntel Silicone Thrombectomy Catheters worldwide because the guide tip can become damaged and detach during use.
Medline Industries is recalling Namic Fluid Delivery Sets (lot 0000113381) because they lack sterility assurance, which could allow contamination during medical procedures.
Baxter Healthcare Corporation has recalled 9 Spectrum IQ Infusion Pumps due to potential cracks on the front panel mount. Units distributed in Ohio and Wisconsin are affected.