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. 2,072 recalls have been distributed to Tennessee in the last 12 months.
Showing 6901–6920 of 52,000 recalls
Recalled Item: Golden Owl Dried Mango 7 oz (200g) . Packaged Recalled by TRUONG GIANG...
The Issue: Undeclared sulfites
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Norepinephrine Bitartrate in 5% Dextrose Injection Recalled by Baxter...
The Issue: Incorrect product concentration on the overwrap label: The overwrap label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System (New and ) Recalled by Ortho-Clinical...
The Issue: Potential For Aspiration from Unintended Sample Container During Sampling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System (New and ) Recalled by Ortho-Clinical...
The Issue: Potential For Aspiration from Unintended Sample Container During Sampling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1...
The Issue: Potential interference with the anti-fall system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head Recalled by...
The Issue: Mislabeled: Packaging incorrectly a MobileLink Dual Mobility insert type F...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT7600 Integrated System Recalled by Ortho-Clinical Diagnostics, Inc....
The Issue: Potential For Aspiration from Unintended Sample Container During Sampling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component...
The Issue: Invacare Homecare & G-Series Bed Components identified with a potential weld...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INS7280 / Integra¿ Cranial Access Kit. For access to the Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE VIABIL Short Wire Biliary Endoprosthesis Recalled by W.L. Gore &...
The Issue: Devices without transmural drainage holes may be mislabeled as devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHRZN / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITH / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.