Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,664 recalls have been distributed to Tennessee in the last 12 months.
Showing 11101–11120 of 29,188 recalls
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streamline TL Navigation System Recalled by RTI Surgical, Inc. (dba Pioneer...
The Issue: The Streamline Navigation System taps have experienced binding with other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streamline MIS Navigation System Taps Recalled by RTI Surgical, Inc. (dba...
The Issue: The Streamline Navigation System taps have experienced binding with other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yuno Mobile Operating Table - Product Usage: Intended for support Recalled...
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: 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: 5.5MM Arthrogarde Hip Access Cannula Recalled by Smith & Nephew, Inc. Due to...
The Issue: The J Lock feature on the cannula body was manufactured incorrectly,...
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.