State
72,984 recalls have nationwide distribution and so reach Kentucky. 7,165 additional recalls listed Kentucky specifically in their distribution scope.
Of the 7,165 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 7,165 recalls whose distribution notice names Kentucky specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.
GE HealthCare SIGNA Architect MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.
Endosee System Convenience Kits are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 991 units are affected.
Budesonide Inhalation Suspension 0.5 mg/2 mL is being recalled for lack of assurance of sterility after a market complaint was received for leakage and an empty ampoule. 13,680 ampoules affected.
Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.
The Azurion 7 M20 fluoroscopic x-ray system is being recalled because of the potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose. 78 units affected.
Endosee System Convenience Kits with IV Tube are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 475 units affected.
Clomipramine Hydrochloride Capsules USP 25 mg are being recalled after an out of specification result for an unspecified degradation product during retention sample testing at expiry. 2,724 bottles affected.
A compounded Tropicamide-Proparacaine-Phenylephrine-Ketorolac sterile ophthalmic solution is being recalled because of subpotent assay results during stability testing. 2,890 vials are affected.
ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses are being recalled because of defects, specifically bubbles and voids, identified during standard finished goods testing. 114,165 lenses affected.
Terran Industries is recalling 7000lb axle assemblies because incorrect suspension components may have been installed, posing a risk of axle spring failure or wheel detachment.
Mack Trucks is recalling 2026 Granite GR trucks because incompatible brake drums and steer axles may cause loss of brake function, increasing crash risk.
Kia is recalling certain 2023-2025 K5 vehicles because the left and right rear window trim pieces may loosen and detach, becoming a road hazard for other vehicles.
Kia is recalling certain 2023-2025 Telluride vehicles because the door belt molding trim can delaminate and detach from the vehicle, becoming a road hazard.
Porsche is recalling 2024-2025 Macan 4 Electric vehicles because front seat air bags may be improperly secured, potentially preventing proper deployment during a crash.
Grech Motors is recalling certain 2020-2025 Strada, Turismo and Terreno motorhomes because the retractable awning may extend unintentionally while the vehicle is moving.
Tesla is recalling certain 2026 Model Y vehicles because the horn ground wire ring terminal may be improperly secured, causing the horn to fail. An inoperable horn increases the risk of crashes.
USDA FSIS issued a public health alert for Reser's and Molly's Kitchen ham salad products containing breadcrumbs recalled for possible Listeria monocytogenes contamination.
Ford is recalling certain 2025 Lincoln Navigator, F-150, Expedition, Bronco and Ranger vehicles because the Electronic Brake Booster module may malfunction, causing a loss of power brake assist.
Mercedes-Benz is recalling certain 2022-2023 EQB 300 and EQB 350 4MATIC vehicles because the high voltage battery bus bar may be secured with incorrect screws, causing a sudden loss of drive power.
Forest River is recalling 2025-2026 Sunseeker, Solera, and other motorhomes because fuel line connectors may detach, creating a fire hazard.
Ford is recalling certain 2025 Lincoln Aviator vehicles because when using the global closing feature, the side rear windows may exert excessive force on an object before automatically reversing.
Ford is recalling specific Bronco Upfit kits because the rearview camera may not display an image, increasing crash risk. Dealers will replace the camera free of charge.