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. 1,110 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,110 in last 12 months

Showing 7281–7300 of 29,188 recalls

Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· NuVasive Inc

Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...

The Issue: Potential that insert will be unable to disengage from the vertebral body...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid q ultrasound. Used in ultrasound imaging and analysis in Recalled by...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Recalled by...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid q N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Recalled by...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S6 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: API LISTERIA 10 STRIPS+10 MEDIA Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK MS CLINICAL REAGENT VITEK MS-DS Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GP78 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM LOMBARD PRODUCTS IRR COUNT-TACT 3P AGAR 100 PLT Recalled by Biomerieux...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL ETEST MEROPENEM MP M100 US Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM CLINICAL CHROMID MRSA 20 PLT US Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30 Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL MINOCYCLINE MC 256 US S30 Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS SALMONELLA 60T Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT Recalled by Biomerieux...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing