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.
Medline is recalling ortho spine, urology minor, set up and hip pinning convenience kits after complaints of anesthesia circuit leaks from cracked tubing. The FDA classified it Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Medline is recalling open heart supplement and vascular kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Tiffin Motorhomes, Inc. is recalling certain 2026 Open Trail motorhomes because the cargo carrying capacity labels may be incorrect, which could lead to vehicle overloading.
Professional Botanicals is recalling 430 bottles of Total Comfort capsules because the product contains magnesium salicylate.
Covidien is recalling two units of a VATS lobectomy box containing the Signia Small Diameter Curved Tip Intelligent Reload because internal components may move during firing.
Applied Medical Technology is recalling NutraGlide 6 F-8 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Siemens Healthcare Diagnostics is recalling 34 units of IMMULITE 2000 Oak Mix Specific Allergen because barcode orientation causes the instrument to misread tube positions in the holder wedge.
Medline is recalling 58,499 reprocessed LigaSure Impact sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.
Shimadzu is recalling 1,766 ceiling type X-ray tube supports, models CH-200 and CH-200M, because the mounting shaft may break and the tube assembly could come off.
Applied Medical Technology is recalling NutraGlide 5 F-6 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Siemens Healthcare Diagnostics is recalling 28 units of Food Panel 3 Specific Allergen because barcode orientation causes the instrument to misread tube positions in the holder wedge.
Blue Oven Bakery is recalling about 4,500 bags of Blue Oven Artisan Bakery English Muffins sold in Indiana, Kentucky and Ohio over undeclared milk.
Medline is recalling 1,446 reprocessed LigaSure Blunt Tip sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.
Olympus is recalling 48,208 Single Use Electrosurgical Snares SD-400 because sterility may be compromised by small holes formed during packaging or transportation.
Olympus is recalling 1,528 ShockPulse Lithotripsy Transducers because the device may fail to start or stop shortly after starting, and the handpiece body may heat up during clinical use.
Orthofix is recalling 624 Virata preassembled polyaxial screws used in the Virata Spinal Fixation System because the screws do not meet performance standards.
Abbott Laboratories is recalling 833 Alinity hq Analyzers because a software issue means the system does not visibly flag results when saturation is present, which may give incorrect results.
Medline is recalling 4,226 reprocessed LigaSure Exact dissectors, 21 cm, because certain areas of the device can trap residual material that may become dislodged.
Medline is recalling 60,917 reprocessed LigaSure Blunt Tip sealer/dividers, 37 cm, because certain areas of the device can trap residual material that may become dislodged.
GE Healthcare is recalling 2,857 FLEX-3S2P lithium-ion batteries used with patient monitors because they can lose the capability to hold charge and provide backup power.
GE Healthcare is recalling 3,271 Carescape B450 patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Covidien is recalling 3,263 Signia Small Diameter Curved Tip Intelligent Reloads because a manufacturing issue can allow internal components to move during firing, risking uncontrolled motion.
Medline is recalling 65 reprocessed LigaSure Blunt Tip sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Medline is recalling one reprocessed LigaSure Impact Curved Large Jaw sealer/divider because certain areas of the device can trap residual material that may become dislodged.