State
73,388 recalls have nationwide distribution and so reach Kentucky. 7,197 additional recalls listed Kentucky specifically in their distribution scope.
Of the 7,197 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 7,197 recalls whose distribution notice names Kentucky specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Launch Sequence Euphoria Capsules have been recalled because the product contains undeclared tadalafil, an unapproved active ingredient. The capsules were distributed nationwide in the USA and Canada.
FDA recalls Ortiga mas Ajo Rey dietary supplement sold nationwide due to undeclared diclofenac. Product marketed as supplement contains pharmaceutical ingredient not listed on label.
The FDA is recalling Artri Ajo King tablets nationwide after finding they contain undeclared diclofenac, a prescription anti-inflammatory drug. Affected bottles (lot LTARTKNGOMG30220, expiring December 2025) were sold on Amazon.
Amazon is recalling Artri King herbal supplement tablets nationwide due to FDA laboratory findings of undeclared diclofenac, a pharmaceutical medication not listed on the label. The product was marketed without FDA approval.
GE Healthcare anesthesia systems may have reversed oxygen and air transducer connections, potentially affecting proper gas delivery. 5,372 devices worldwide are affected.
Volkswagen is recalling 1,216 2016 Audi and Volkswagen vehicles because the front passenger air bag may explode or deploy improperly, posing a risk of serious injury or death.
Launch Sequence Aphrodisia Capsules contain undeclared tadalafil, making them an unapproved drug. The recall involves 500 4-count tins distributed nationwide in the USA and Canada.
Launch Sequence Capsules dietary supplement recalled for containing undeclared tadalafil, an FDA-approved pharmaceutical ingredient. The product was marketed without required drug approval.
Queen Bee Gardens recalls Honey Caramels Strawberry Lemonade due to undeclared tree nuts. The product may contain pecans, almonds, coconut, macadamia nuts, or walnuts, posing a risk to consumers with tree nut allergies.
Loud Muscle Science is recalling Launch Sequence Aphrodisia Capsules because they were marketed without FDA approval. The product was distributed nationwide in the USA and Canada.
Nephron Sterile Compounding Center is recalling Neostigmine Methylsulfate Injection due to lack of assurance of sterility. The recall affects 10,700 syringes distributed nationwide.
Queen Bee Gardens is recalling English Toffee Milk Chocolate and related products containing undeclared tree nuts. Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Queen Bee Gardens is recalling Black Forest Classic Truffle chocolates that may contain undeclared tree nuts not listed on the label.
Nephron Sterile Compounding Center recalls Lidocaine HCl Injection 2% syringes distributed nationwide due to lack of assurance of sterility. Affected lots should not be used.
Queen Bee Gardens is recalling All Milk Classic Truffles (1.4 oz) because they may contain undeclared tree nuts, posing a risk to consumers with tree nut allergies.
Certain Hill-Rom PRO+ MRS mattresses may have a Microclimate Management feature failure that increases patient pressure ulcer risk. Affected units were distributed to 25+ U.S. states and Canada.
Micro Bird is recalling 2021-2022 G5, MB II, and T-Series school buses because window panels may detach in a crash.
Queen Bee Gardens is recalling Honeymoon Patties Mint Bee Patties because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). The product was sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Baxter Healthcare is recalling 404 Hill-Rom PRO+ 36" mattresses due to performance degradation in their heat and moisture management feature. This failure increases the risk of pressure ulcer development in patients.
Queen Bee Gardens is recalling QBee Honeycomb Toffee Milk due to undeclared tree nuts. Consumers with tree nut allergies face a potential allergic reaction risk.
GE Healthcare's SIGNA Premier MRI scanner is being recalled because under rare conditions, the gradient coils can produce elevated acoustic noise that could potentially cause hearing loss with prolonged exposure.
Queen Bee Gardens is recalling Honey Caramels Red Raspberry because the product may contain undeclared tree nuts. The recalled items were distributed to Queen Bee retail stores in Colorado, New Mexico, and Wyoming, and nationwide via internet sales.
Aesculap is recalling AESCULAP S4 Cervical Cross Connectors used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to loosen or shift on the spinal rods.
Becton Dickinson is recalling certain BD Connecta Plus1 360 Blue Blend infusion connectors due to potential leakage at the housing stopcock that could interrupt treatment and expose patients to contamination and biohazardous material.
Queen Bee Gardens is recalling Honeymoons Dark Chocolate Almond for undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product was distributed to retail locations in Colorado, New Mexico, and Wyoming, and nationwide online.