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.
Showing 8141–8160 of 52,000 recalls
Recalled Item: VITROS Chemistry Products Lipase Slides Recalled by Ortho-Clinical...
The Issue: Products 1668409 and 8297749 may contain VITROS Lipase Slides with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System Recalled by...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare 5B and 6A including service packs- An oncology information Recalled...
The Issue: An issue was found in RayCare 5B, 6A, including service packs, where values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The firm has investigated and confirmed that when DxI 9000 is connected to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Plus Aerobic/F Culture Vials Recalled by Becton Dickinson & Co....
The Issue: Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LittleOak Natural Goat Milk Follow On Infant Formula (Stage 2) Recalled by...
The Issue: No pre-market notification and Mixing instructions not in ounces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LittleOak Natural Goat Milk Infant Formula (Stage 1) Recalled by The Little...
The Issue: No pre-market notification and Mixing instructions not in ounces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.