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. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 27441–27460 of 52,000 recalls
Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn, Inc. Due to Subpotent...
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...
The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IGS 730 Interventional Fluoroscopic X-ray Systems Recalled by GE...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...
The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IGS 740 Interventional Fluoroscopic X-ray Systems Recalled by GE...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...
The Issue: There is a potential for debris in the hole on the superior lateral aspect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conzerol zero molluscum contagiosum Recalled by Elroselabs Inc. Due to cGMP...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Molleave Recalled by Elroselabs Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Conzerol (antipoxin) H2O2 Gel Recalled by Elroselabs Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The dose calculation accuracy may in some situations be less than expected....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...
The Issue: Software anomaly resulting in the loss of patient settings and stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.