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. 2,652 recalls have been distributed to Kentucky in the last 12 months.
Showing 4641–4660 of 51,386 recalls
Recalled Item: STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to Recalled by B...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW Real Foods Whole & Unsalted Raw Brazil Nuts 12oz. bag Recalled by Now...
The Issue: High mold, yeast, and total viable count
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TxHA PEEK IBF/TxTiHA IBF System i. TxHA The Recalled by Innovasis, Inc Due...
The Issue: Due to interfacing issues between the implant trial and inserter of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium SuperPulsed Laser - Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser Systems-Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective Container: patients are unable to get the solution out of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Custom Procedure Kit Recalled by Merit Medical Systems, Inc. Due to 7F...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Sheath Introducer 7.5F Recalled by Merit Medical Systems, Inc. Due...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Seer Home System is an ambulatory electroencephalograph (EEG) system...
The Issue: During CAPA investigations of sight production inconsistencies, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (narrow indication)-Intended for...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Food brand Steam Bun with Egg Custard & Coconut Added Recalled by...
The Issue: Products may contain undeclared sesame
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prime Food brand Steam Bun with Egg Custard Added Recalled by Prime Food...
The Issue: Products may contain undeclared sesame
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ibuprofen 800mg Recalled by Direct Rx Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: Product failed impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vios Monitoring System Bedside Monitor Model BSM2050 Recalled by Murata...
The Issue: Batteries may deplete over time while not in use if devices are stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILIZABLE INTERNAL DEFIBRILLATION PADDLES STERILIZABLE INTERNAL...
The Issue: Due to customer complaints and out of box failures, the firm is conducting a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Gel Recalled by Teva Pharmaceuticals USA, Inc Due to...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fusion Pro 24 Recalled by Epilog Laser Corp. Due to a. A small number of...
The Issue: a. A small number of Fusion Pro 24 units were released with an incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAILIES TOTAL1 Recalled by Alcon Research LLC Due to Material with a quality...
The Issue: Material with a quality issue was used in contact lens production, so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eakin Cohesive seal Recalled by T.G. Eakin Limited Due to On lot of cartons...
The Issue: On lot of cartons of Eakin Cohesive small seals, Model Number 839002 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.