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. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22281–22300 of 29,188 recalls
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: The Centricity...
The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...
The Issue: DLS pin breakage during planned implant removal, after uneventful and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver Recalled by...
The Issue: The RASH3N, a hexed, abutment screw driver tip has been labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips Recalled by...
The Issue: RASQ3N, a square, abutment screw driver tip has been labeled and distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cadiere Forceps Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crocodile Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fenestrated Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medium -Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maryland Dissector Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fundus Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Vascular Loop Catalog Number CH111 Recalled by International Biophysics...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a...
The Issue: Software defect that impacts image alignment when using the automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Recalled by...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Aortic Punch Catalog Numbers APM40 Recalled by International Biophysics...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI 500 Blood Parameter Monitoring System. Provides continuous Recalled by...
The Issue: Inaccuracies in SvO2, temperature, pH, pCO2, pO2, Hematocrit, and Potassium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.