State
73,198 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 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Navistar is recalling 2024 IC Bus CE school buses because steering gear assemblies may have fewer recirculating balls than required, risking loss of steering control.
Husqvarna is recalling about 403,000 gas-powered grass trimmers due to incorrect wiring in the ignition module that can cause electrical sparks or arcing, creating a fire hazard. The firm has received 12 reports of fires, including one burn injury.
Daimler Trucks North America is recalling 2022-2024 Western Star 49X vehicles with suspension hangers that may fail due to missing welds, potentially impairing steering and directional control.
CableMod GPU V1.0 and V1.1 angled adapters can overheat and melt, posing fire and burn risks. The firm has received 272 reports of overheating with at least $74,500 in property damage, though no injuries have been reported.
GM is recalling 338 2024 Chevrolet Silverado EV vehicles due to an incorrect second-row center seat belt bezel that may damage or tear the seat belt in a crash, potentially failing to restrain occupants.
General Motors is recalling Autoliv driver front air bags sold as service replacement parts for 2011-2012 Chevrolet Silverado 1500, Suburban, and Tahoe vehicles due to a manufacturing defect.
Electrolux Group is recalling about 383,240 Frigidaire side-by-side refrigerators with slim ice buckets because the ice bucket assembly can break and release plastic pieces that pose choking and laceration hazards.
EarthRoamer is recalling 2022-2023 LTi motorhomes because a control module may cause fuel to overflow and leak, increasing fire risk.
Braun Ambulances is recalling 2023-2024 models because a lighting control module defect may cause turn signals, brake lights, and backup alarms to fail, increasing crash risk.
Lolanta children's hooded flannel bathrobes violate federal flammability regulations for children's sleepwear and pose a burn hazard. About 16,900 units were sold online from January 2021 through October 2023.
Ford is recalling certain 2023 Explorer vehicles with a loose or missing fastener in the front suspension. This can cause steering pull and brake failure, increasing crash risk.
USDA FSIS issued a public health alert for ready-to-eat poultry products containing dairy recalled for possible Listeria monocytogenes contamination.
VPR Brands is recalling about 62,200 disposable lighters (Slim Soft and Slim Jet models) sold between September 2022 and November 2023 because they lack child-resistant mechanisms required by federal regulation, posing fire and burn hazards to young children under 5.
Denver Solutions is recalling 29,016 Phenylephrine HCl IV bags distributed nationwide. A filling system malfunction can result in some bags receiving double doses of this potent injectable drug.
Denver Solutions is recalling 7,548 IV bags of vancomycin due to a manufacturing system malfunction that can deliver double doses. The product was distributed nationwide.
The FDA has recalled Zenzedi (Dextroamphetamine Sulfate) 30 mg tablets due to a labeling error. The recall affects 4,662 bottles distributed nationwide.
Denver Solutions recalled 8,976 IV bags of fentanyl citrate nationwide due to a malfunction in the semi-automated filling system that could deliver double the intended dose.
Suzuki is recalling 2024 GSX-8R motorcycles because the drive chain may detach due to missing rivets, which can cause a loss of power to the rear wheels and increase crash risk.
Denver Solutions is recalling 10,152 Vancomycin IV bags nationwide because a filling system malfunction can deliver double doses of the antibiotic medication.
Olympus recalls EZDilate Wire Guided Balloon devices used for endoscopic dilation due to reported bursting, leaking, and retrieval failures affecting 1,639 units nationwide.
Olympus is recalling 2,991 EZDilate endoscopic balloons for problems with inflation and deflation. Reports include device bursting and leaking, and retained foreign bodies in patients during procedures.
Olympus is recalling approximately 6,898 EZDilate Wire Guided Balloon devices due to reported bursting, leaking, and retrieval problems during medical procedures.
Olympus recalled 3,354 EZDilate wire-guided dilation balloons due to failures in inflation, deflation, and retrieval, with incidents of bursting, leaking, and foreign bodies left in patients.
FentaNYL citrate intravenous bags are recalled nationwide because a semi-automated filling system can malfunction and deliver double the intended dose. Patients and healthcare providers should immediately quarantine affected lots.
The FDA is recalling Smiths Medical Medfusion Model 4000 syringe pumps due to software defects affecting medication delivery, alarms, and display accuracy. Users should install the latest software version to correct these issues.