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. 2,509 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,509 in last 12 months

Showing 2456124580 of 29,188 recalls

Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Recalled...

The Issue: Sterility of device is compromised due to breach in sterile barrier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus...

The Issue: Springs contained in the access door hinge assembly on the Walk Away Plus...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Ability Dynamics LLC

Recalled Item: RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use Recalled...

The Issue: Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing Recalled...

The Issue: Swollen acid bottles due to a trace metal contamination in the Acid Reagent...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems TnI-Ultra assay Recalled by Siemens Healthcare...

The Issue: The solid phase reagent in some of the ADVIA Centaur¿ TnI -Ultra...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Carestream Health Inc.

Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...

The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP Calibrators for the Beckman Coulter Access Family Recalled...

The Issue: Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 29, 2014· Synthes, Inc.

Recalled Item: Synthes Guide Blocks for the 2 Column Plate 6 Hole Recalled by Synthes, Inc....

The Issue: The Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing