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. 1,820 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,820 in last 12 months

Showing 3236132380 of 52,000 recalls

FoodDecember 16, 2016· Berner Food & Beverage, LLC

Recalled Item: Lite Creamy Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...

The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 16, 2016· Berner Food & Beverage, LLC

Recalled Item: Roasted Garlic Alfredo Recalled by Berner Food & Beverage, LLC Due to...

The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 16, 2016· Berner Food & Beverage, LLC

Recalled Item: Creamy Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...

The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 16, 2016· Berner Food & Beverage, LLC

Recalled Item: Our Family Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...

The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 16, 2016· Berner Food & Beverage, LLC

Recalled Item: Four Cheese Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...

The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 16, 2016· Parker Medical

Recalled Item: Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker...

The Issue: The product was not functioning as intended. The ventilation to the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The AMM Recalled...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension AMM (DF119)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista AMM...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Covidien LLC

Recalled Item: Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10 Recalled by Covidien...

The Issue: Labeling error: The label indicates the product is latex free, but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy...

The Issue: An error can occur causing Delta corrections to be lost when one setup field...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT with software version 4.7.0 Product Usage: The Recalled by...

The Issue: Multiple issues have caused the device to result in CT rescans or incorrect...

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

Class II — Potential Health HazardOngoing
FoodDecember 15, 2016· Arcadia Trading Inc.

Recalled Item: LIZARD FISH (Eviscerated) Recalled by Arcadia Trading Inc. Due to The...

The Issue: The imported Lizard Fish was found to be uneviscerated based on FDA sampling...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Doripenem DOR32 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Ceftriaxone TXL32 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Vancomycin VA 256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Ceftazidime TZ256 Foam packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Gentamicin GM256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: Ciprofloxacin CI 32 Foam packaging Recalled by BioMerieux SA Due to Product...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Cephalotin CE 256 Foam packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Benzyl Penicillin PG256 FOAM packaging Recalled by BioMerieux SA Due...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing