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. 2,637 recalls have been distributed to Tennessee in the last 12 months.
Showing 14701–14720 of 29,188 recalls
Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Oncology Kit w/12" (30cm) Ext Set w/Spiros w/Red Cap Recalled by...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoLock Recalled by ICU Medical, Inc. Due to There is a...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Oncology Kit w/12" Ext Set w/Spiros w/Red Cap Recalled by ICU...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD...
The Issue: BD Synapsys version 2.1 allowed the potential for a test order to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES C. difficile Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Flu A/B & RSV Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES GBS Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Group A Strep Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aries Bordetella Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Extraction Kit Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS ECi Immunodiagnostic System Product Code: 6801059 For use Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald analyzer Recalled by Abbott Laboratories Due to There is a...
The Issue: There is a potential for the device to generate Quality Control (QC) low or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.