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. 2,646 recalls have been distributed to Kentucky in the last 12 months.
Showing 5621–5640 of 28,748 recalls
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sapphire Infusion Pumps Recalled by EITAN MEDICAL LTD Due to Infusion Pumps...
The Issue: Infusion Pumps with affected software revision may fail to detect air in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Viewer Workflow Manager Recalled by GE Healthcare Due to When...
The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Workflow Manager Recalled by GE Healthcare Due...
The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...
The Issue: There is a potential interruption of data communication between E-modules...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software...
The Issue: CORI software was missing a planning stage that appears in cases of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSP Glenoid Baseplate Recalled by Encore Medical, LP Due to Coating hex did...
The Issue: Coating hex did not engage with the Straight Mod Hexdriver or with the Hex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...
The Issue: The firm has identified that the Transferrin reagent does not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000 Recalled by...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000 Recalled by...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R ()...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number:...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. W/O CDX BLUESTAR Recalled by Fresenius Medical Care Holdings,...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis SYS Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. W/O CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T GEN 2 Bibag without CDX Recalled by Fresenius Medical Care Holdings,...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.