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 11041–11060 of 28,748 recalls
Recalled Item: Yuno II Mobile Operating Table - Product Usage: support and Recalled by...
The Issue: Plastic socket of the IEC 60320-1 socket pulled out of the metal cage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVu Single Use Video Stylet with ET Tube Recalled by Flexicare Medical...
The Issue: When the video stylet cuff is over-inflated there is potential for occlusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kangaroo Connect 1000ml Bag Set Recalled by Cardinal Health 200, LLC Due to...
The Issue: The feeding spike sets may leak at the interface of the tube and spike...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kangaroo Connect 500ml Bag Set Recalled by Cardinal Health 200, LLC Due to...
The Issue: The feeding spike sets may leak at the interface of the tube and spike...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TroClose 1200 - Product Usage: intended for use in a variety of gynecologic...
The Issue: Endotoxin test results found above the acceptable levels in LAL test (above...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal) Recalled by Pentax...
The Issue: There is an intermittent software issue that could affect the systems, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visual-ICE MRI Cryoablation System Mobile Connection Panel (Visual-ICE MRI...
The Issue: Incorrectly installed base.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9310HD Digital Video Capture Module with software version 3.4.0 or Recalled...
The Issue: There is an intermittent software issue that could affect the systems, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Niobe ES System Recalled by Stereotaxis Inc Due to There is a potential for...
The Issue: There is a potential for fire in the inside computer cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to There is a potential...
The Issue: There is a potential for a smudge artifact that could be suspect for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...
The Issue: Potential malfunction in which the examination room monitor may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Increase...
The Issue: Increase in fracture complaints of the flexible, tapered core wire,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis (GII) - Product Usage: designed for use in patients Recalled by...
The Issue: The anterior locking detail does not meet its design specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...
The Issue: There is a software problem which affects the DSA Roadmap application on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....
The Issue: Device malfunction causing the applier to jam, and clip loading failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.