State
72,940 recalls have nationwide distribution and so reach Kentucky. 7,164 additional recalls listed Kentucky specifically in their distribution scope.
Of the 7,164 recalls naming Kentucky we have scored against our rubric, 1,399 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,694 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,164 recalls whose distribution notice names Kentucky specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2025-2026 Mustang Mach E vehicles because a software defect may prevent exterior lights from working, increasing crash risk.
International Motors is recalling 2026-2027 IC Bus CESB school buses because wheelchair retractors may not lock, increasing injury risk.
Altec is recalling certain 2023-2025 Aerial Device and Digger Derrick vehicles because the electronic taillight module harness may have inadequate circuit protection.
Ford is recalling certain 2021-2022 Bronco vehicles previously repaired under recall 23V165, because the rearview camera image may still be displayed after a backing event has ended.
Ford is recalling certain 2025 and 2026 Maverick vehicles because the instrument panel cover may separate during an airbag deployment, potentially striking occupants and increasing injury risk.
General Motors is recalling 2025–2026 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not produce sufficient volume change between stopped and low-speed operation, failing to meet federal safety standards.
Honda is recalling 2024–2026 CBR600RR motorcycles because the cylinder head may have been improperly manufactured, risking rear wheel lockup and engine fire.
About 12,000 JOKOSIS portable bed rails, model HC0262, are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 80 SereneLife above-ground pools 48 inches and taller, models SLPORND15 and SLPORND18, are being recalled because a compression strap may create a foothold allowing a child to access the pool.
About 50,330 jars of Mamisan Pain Relieving Topical Ointment are being recalled because the ointment contains lidocaine and the packaging is not child-resistant.
About 650 Schwinn Ovation Bicycle Child Carriers are being recalled because the buckles securing the restraints around the child can release during use, posing a fall hazard.
About 2,800 17 Stories Furniture 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 11,200 ANNQUAN power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded.
About 840 bottles of Feel The Beard Minoxidil Beard Growth Oil are being recalled because the product contains minoxidil and the packaging is not child-resistant.
About 260 Currey & Company Electra chandeliers are being recalled because the component connecting the fixture to the ceiling mount is not threaded properly and the fixture can fall.
Ford is recalling 2019 Expedition vehicles previously repaired under recall 20V263 because the 'Transmission Not In Park' warning message and chime are shorter than intended.
Chetak New York is recalling Deep-brand frozen tindora after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 13,069 cases of 4 lb Peppermint Peach white peaches over potential contamination with Listeria monocytogenes.
Moonlight Packing is recalling 104 cases of 2 lb bagged white peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen hot green chillies after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen sambhar mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 570 cases of 2 lb Peppermint Peach bags over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling 439 bags of 4-count Peppermint Peach packs over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling 2,603 cases of loose bulk peppermint peaches over potential contamination with Listeria monocytogenes, under enforcement record H-0323-2026.
ByHeart is recalling 3,482,131 cans and 3,531,901 single serve packets of Whole Nutrition Infant Formula after contamination with Clostridium botulinum. The FDA has classified the action as Class I.