State
73,478 recalls have nationwide distribution and so reach Kentucky. 7,202 additional recalls listed Kentucky specifically in their distribution scope.
Of the 7,202 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 2,024 (28%) are Severe.
Which agencies issued them
These figures cover only the 7,202 recalls whose distribution notice names Kentucky specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling certain 2022 Chevrolet Silverado and GMC Sierra trucks with an accessory sport bar. The high-mounted brake light may not function or may be blocked, reducing visibility to other drivers and increasing crash risk.
Yamaha is recalling about 3,500 Model Year 2021 and 2022 Kodiak 700 ATVs because they are missing the "Maximum Loading Limit" label, which can result in unsafe trailer towing and crash hazards.
Calico Cottage Inc is recalling Peanuttiest Caramel Chocolate fudge nationwide because the peanut butter ingredient may be contaminated with Salmonella.
Calico Cottage Inc is recalling peanut butter fudge products due to potential Salmonella contamination in the peanut butter ingredient. The recall affects bulk carton products distributed nationwide.
Smiths Medical recalled 58,671 Medfusion Syringe Pump units worldwide due to multiple failures that could interrupt therapy or cause over-infusion, including defective alarms and display errors.
Albanese Confectionery Group recalls Rich's Milk Chocolate peanut butter cups nationwide due to Salmonella contamination from recalled Jif peanut butter used in manufacturing.
Calico Cottage Inc is recalling chocolate fudge products containing peanut butter due to potential Salmonella contamination. The recall affects 677 units distributed nationwide.
Smiths Medical is recalling multiple Medfusion Syringe Pump models due to software and hardware defects that may interrupt drug infusion or cause over-infusion. Approximately 65,093 units distributed worldwide are affected.
Medtronic is recalling HeartWare HVAD batteries (Model 1650DE) due to an internal weld defect that can cause battery malfunction and prevent proper charging. Approximately 429 affected batteries were distributed worldwide.
Calico Cottage Inc is recalling Salted Nut Roll Pre-Made Fudge nationwide because the peanut butter ingredient is potentially contaminated with Salmonella.
Olympus Corporation recalls a single colonovideoscope model CF-H180AL because an incorrect camera unit was installed, causing narrower viewing angle and potential device protrusion that could injure tissue. No injuries have been reported.
Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.
Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.
Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.
Taylor Farms is recalling Trader Joe's BBQ & Black Pepper Toscano Chopped Salad because it contains undeclared peanuts and peanut lime dressing due to an incorrect master pack. The product poses a risk to consumers with peanut allergies.
Red Button Vintage Creamery Canadian Vanilla Ice Cream was distributed nationwide with undeclared almond allergen due to packaging mix-up. Consumers with tree nut allergies should not consume this product.
Bard Peripheral Vascular Inc is recalling certain catheter drainage kits that may contain an 8 Fr needle instead of the correct 6 Fr needle. The incorrect needle size could cause tissue injury during patient care.
EarthLab Inc is recalling Wise Woman Herbals Standardized Kava Glycerite due to high yeast and mold counts detected during microbial testing. The affected product was distributed nationwide.
Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.
Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets (0.125mg) due to manufacturing defects where oversized tablets were found. The affected lot (MHC1430A, exp. 09/2023) was distributed nationwide.
Beaver Visitec International recalled 660 units of BVI Wet-Field Eraser surgical devices after discovering boxes labeled with one tip configuration contained a different tip design. This mismatch could affect surgical precision and hemostasis control.
Alcon is recalling specific lots of Clareon intraocular lenses (IOLs) due to mislabeling caused by improper manufacturing line clearance. The mislabeling resulted from partial product mixing during overlapping manufacturing runs.
KZRV is recalling 2021 Escape travel trailers because the tire placard lists incorrect information, which can lead to overinflated tires and increased crash risk.
Maquet Cardiovascular recalls INTERGARD Woven Vascular Grafts with incorrect labeling. Units labeled as 8 mm diameter instead contained 32 mm diameter grafts.
CardioTek EP-TRACER Software V2.x is recalled because it failed electrical safety testing for insulation. The 146 affected units were distributed worldwide.