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. 1,056 recalls have been distributed to Tennessee in the last 12 months.
Showing 16721–16740 of 52,000 recalls
Recalled Item: BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 VR-T DX Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 VR-T Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 cm Recalled by Arrow...
The Issue: Difficulty inserting the biopsy ejector rod into the bone lesion biopsy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VEGAN VITAMIN D3 Recalled by New Generation Wellness Inc. Due to Vitamin D3...
The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Live Better vegan vitamin d-3 by CVS Health Recalled by New Generation...
The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) Dual Aspirate Autosampler (SMN 11219530) - US Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodisc C - prosthesis Recalled by Centinel Spine, Inc. Due to Centinel...
The Issue: Centinel Spine learned through five customer complaints that the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Dual Aspirate (SMN 11314045) - OUS Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 SAA AUTOSAMPLER (SMN 10374453) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - OUS...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Dual Aspirate (SMN 11314045) - US Recalled by Siemens Healthcare...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Dual Aspirate Autosampler (SMN 10285573) - OUS Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 DAA AUTOSAMPLER (SMN 10374454) - OUS Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Dual Aspirate Autosampler (SMN 10285573) - US Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) Dual Aspirate Autosampler (SMN 11219530) - OUS Recalled...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter...
The Issue: The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - US...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.