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. 1,937 recalls have been distributed to Kentucky in the last 12 months.
Showing 16621–16640 of 51,386 recalls
Recalled Item: Ultrasonic pulsed doppler imaging system - Product Usage: intended for...
The Issue: Arietta 850 software version 4.0.0., 4.0.1, and 4.0.2 has an error in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg Recalled by Alvogen,...
The Issue: Subpotent drug: Out of specification for assay of naloxone and buprenorphine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: tastebuds Taco Dip Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: tastebuds Taco Platter Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Haug Fresh Mini 7 Layer Dip Tray Recalled by J & J Distributing Company Due...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Dip [Kwik Trip] Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresh Thyme Taco Dip Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Haug Fresh Taco Tray Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Earthgrown Mini Taco Dip Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caribou Coffee Turkey Sandwich Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Platter [Kwik Trip] Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: tastebuds Layered Fiesta Taco Dip Recalled by J & J Distributing Company Due...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Electrolit Fruit Punch Zero Recalled by Laboratorios Pisa Sa De Cv Due to...
The Issue: Product contains undeclared FD&C Red No. 40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Electrolit Ponche/Fruit Punch Recalled by Laboratorios Pisa Sa De Cv Due to...
The Issue: Product contains undeclared FD&C Red No. 40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe HVAD Controller Connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe Expected Alarm Duration. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...
The Issue: Their is a potential that Video Processor/Illuminators may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to There is a...
The Issue: There is a potential for tube trays to leak which could potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.