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. 1,080 recalls have been distributed to Kentucky in the last 12 months.
Showing 12321–12340 of 51,386 recalls
Recalled Item: Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ) Recalled by Fudgeamentals LLC...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. Recalled by...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz. Recalled by Fudgeamentals LLC Due...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PEANUT BUTTER FUDGE BAR (24-8OZ) FUDGEAMENTALS Recalled by Fudgeamentals LLC...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS Recalled by Fudgeamentals...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tegsedi (inotersen) Injection 284 mg/1.5 mL Recalled by Akcea Therapeutics,...
The Issue: Superpotent: High Out of specification (OOS) test result for percent label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MiniMed 640G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 780G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CustMbite Recalled by Dental Choice Holding Llc Due to The device was...
The Issue: The device was marketed and sold in the US without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 670G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 740G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G Insulin Pump (U.S. and Canada Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 620G Insulin Pump (O.U.S. version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 720G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 770G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peanut Butter Pie Recalled by Desserts by Helen, Inc. Due to Product...
The Issue: Product contained JIF peanut butter and was manufactured during the JIF...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System...
The Issue: Potential for stent dislodgement and associated failures related to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Icono Recalled by Siemens Medical Solutions USA, Inc Due to During...
The Issue: During system tests, an increased wearing of the Image acquisition system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Item Number: 800774001 Recalled by ROi CPS LLC Due to A nonsterile...
The Issue: A nonsterile component was packaged in a sterile convenience kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.