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 2508125100 of 29,188 recalls

Medical DeviceApril 14, 2014· Microline Surgical

Recalled Item: Microline Renew Fenestrated Control Tip Grasper Recalled by Microline...

The Issue: Grasper jaw may break when force is applied to the jaw

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Tenex Health Inc

Recalled Item: TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box)...

The Issue: The sterile barrier in the packaging may be compromised due to cracks in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Healthcare Diagnostics Vista Air Compressor. Vista AirCompressor...

The Issue: A small number of Vista Air Compressors were miswired, which if installed...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...

The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...

The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Luminos dRFsystem The Axiom Luminos dRF is intended to Recalled by...

The Issue: It was determined that under rare environmental conditions (i.e., extremely...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Synthes, Inc.

Recalled Item: Synthes External Fixation Systems (Small Recalled by Synthes, Inc. Due to...

The Issue: Labeling changes have been made related to MR (Magnetic Resonance imaging)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Bicarbonate Concentrate Recalled by Fresenius Medical Care...

The Issue: Naturalyte Liquid Bicarbonate maybe contaminated

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD Total 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 500 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Recalled by Siemens Healthcare Diagnostics,...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS Recalled by Siemens...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Potential for biased...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing