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. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1318113200 of 29,188 recalls

Medical DeviceOctober 7, 2019· Nova Ortho-Med Inc

Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...

The Issue: Walkers within the identified serial range have the potential for the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Edwards Lifesciences, LLC

Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...

The Issue: Intermittent communication due to inconsistent crimping of connectors onto...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Implant Direct Sybron Manufacturing LLC

Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Some dental implant packages contain incorrect implants, which could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Beckman Coulter, Inc.

Recalled Item: UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Recalled...

The Issue: When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...

The Issue: Software issue identified in the software versions syngo CT VB20 running on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Smith & Nephew, Inc.

Recalled Item: LAG SCREW 3.2MM GUIDE PIN SLEEVE Recalled by Smith & Nephew, Inc. Due to LAG...

The Issue: LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Ventana Medical Systems Inc

Recalled Item: Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System...

The Issue: The firm became aware of a cleaning solution leaking issue from the middle...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...

The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Teleflex Medical

Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...

The Issue: Certain clip appliers have an increase in misloading and/or jamming related...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Teleflex Medical

Recalled Item: WECK AutoEndo5 Recalled by Teleflex Medical Due to Certain clip appliers...

The Issue: Certain clip appliers have an increase in misloading and/or jamming related...

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

Class II — Potential Health HazardOngoing