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. 2,609 recalls have been distributed to Kentucky in the last 12 months.
Showing 10681–10700 of 28,748 recalls
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...
The Issue: There is the potential for the compounding system to not immediately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON 1-84 PTH Assay - Product Usage: is an in Recalled by Diasorin Inc....
The Issue: Potential for system to produce falsely elevated parathyroid hormone (PTH)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...
The Issue: Device has the potential for fracture during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...
The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 18.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medisafe Distal Duck Kit and Duck Bag Recalled by Steris Corporation Due to...
The Issue: STERIS has identified that certain lots of diluted 4-Zyme may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The cobas z 480 analyzer including dedicated software for IVD Recalled by...
The Issue: Dirty Lens May Cause Invalid or False Positive Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emission Computed Tomography System Image Process System - Product Usage:...
The Issue: A software defect that has the potential to result in image misdiagnosis and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 12.0MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic Recalled by...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 14.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 11.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.