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. 2,670 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,670 in last 12 months

Showing 72817300 of 29,188 recalls

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 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· 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 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· 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 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 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid i 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: ETEST CLINICAL AMIKACIN AK 256 US S30 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-GN80 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 TSA 10PLT 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: VIDAS CLINICAL VIDAS LISTERIA 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: VIDAS CLINICAL VIDAS HCG 60 TESTS 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 INDUSTRY COMBOURG CHROMID CARBA US 20 PLT Recalled by Biomerieux Inc Due...

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 RIFAMPICIN RI 32 US S30 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-N801 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: BIOBALL B.SPIZIZENII NCTC 10400 550X20 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: ETEST CLINICAL MEROPENEM MP 32 US S30 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: ETEST CLINICAL ERAVACYCLINE ERV US S30 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: ETEST CLINICAL COLISTIN CO 256 US B100 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: ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30 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