State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips is recalling 5 of the Azurion 7 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Medline is recalling 2,448 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Asteria Health is recalling 1,699 pellets of ESTRADIOL, 18 mg sterile pellets over the potential presence of metal particulate matter.
Medline is recalling 7,570 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Philips is recalling 1 of the Azurion 7 B20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Asteria Health is recalling 1,758 pellets of Testosterone, 62.5 mg sterile pellets over the potential presence of metal particulate matter.
Intuitive Surgical is recalling 47 da Vinci 5 Surgeon Console Viewer Displays manufactured with outdated firmware, which may cause loss of the 3D surgical field or complete visualization loss.
McCain Foods USA is recalling 21,557 cases of Ore-Ida Tater Tots shaped potatoes over foreign material described as small hard plastic fragments.
Philips is recalling 922 units of the Azurion 5 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Medline is recalling 8,445 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
MG Foods-Compass Group is recalling 3,099 Spicy Breakfast Burritos, 10 oz, over foreign material described as small hard plastic fragments.
Asteria Health is recalling 89,074 pellets of Testosterone, 25.0 mg sterile pellets over the potential presence of metal particulate matter.
Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.
Philips is recalling 3 units of the Spectral CT 7500 on Rails because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Pro Numb Tattoo Numbing Spray LLC is recalling Pro Numb Tattoo Numbing Spray For Sensitive Skin, 4% Lidocaine, over cGMP deviations.
Steris is recalling 10 units of the Barco MNA with HexaVue IP Integration System because the supplier used the incorrect configuration file for a limited batch of adapter components.
Alphatec Spine is recalling 15 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Alphatec Spine is recalling 7 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Laerdal Medical is recalling 1,202 Compact Suction Unit 4 RTCA units because those made in a limited period may emit electromagnetic noise beyond the acceptable RTCA limits.
Domino Foods is recalling 2,023 cases of Sodexo Stars Saccharin (Pink) Packets over undeclared aspartame.
Meitheal Pharmaceuticals is recalling 16,477 Cetrorelix Acetate for Injection kits over a defective delivery system, with needles either missing from or duplicated within the kit.
Unichem Pharmaceuticals USA is recalling 60,000 Doxazosin Tablets, USP 4 mg, because the tablets are imprinted with the wrong ID.
Pro Numb Tattoo Numbing Spray LLC is recalling Pro Numb Tattoo Numbing Spray, 5% Lidocaine, over cGMP deviations.
Straumann USA is recalling 561 WB Impression Post Closed Tray units because the impression caps provided in the package are magenta instead of brown.