Product Recalls in Kentucky
Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 934 recalls have been distributed to Kentucky in the last 12 months.
Showing 44461–44480 of 51,386 recalls
Recalled Item: ROYAL PHARMACEUTICALS DermOtic Oil fluocinolone acetonide 0.01% (Ear Drops)...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops Recalled by Hill...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil)...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% (Scalp...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Creation Special Snack Mix Recalled by Dayton Nut Specialties Inc Due to Due...
The Issue: Due to the lack of the ingredient statement the firm failed to declare the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bar Star Snack Mix Recalled by Dayton Nut Specialties Inc Due to Due to the...
The Issue: Due to the lack of the ingredient statement the firm failed to declare the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bar Star Snack Mix Recalled by Creation Gardens Due to During an inspection...
The Issue: During an inspection by the Kentucky Department for Public Health, the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Creation Special Snack Mix 25 lb plastic bags in a Recalled by Creation...
The Issue: During an inspection by the Kentucky Department for Public Health, the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to The connection between...
The Issue: The connection between the beeper subassembly and the pump may fail. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otto Bock Aerial and Aerial Active Wheelchair Cushions. Material numbers:...
The Issue: Otto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET PLEGIOX Cardioplegia Heat Exchanger The PLEGIOX Cardioplegia Heat...
The Issue: The MAQUET post-marketing vigilance program has identified a discrepancy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Battery Powered Driver Recalled by Synthes, Inc. Due to The CMF...
The Issue: The CMF Battery Powered Driver graphic case contains outlines of the Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001US: Prevena Peel and Place System Kit (US-ONLY) Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2055: Prevena Customizable Dressing 5-Pack Product Usage: The Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1055: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2055US: Prevena Customizable Dressing 5-Pack (US-ONLY) Product Usage: The...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2001: Prevena Incision Management Customizable System Box Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001: Prevena Peel and Place System Kit Product Usage: The Recalled by...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.