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. 2,504 recalls have been distributed to Tennessee in the last 12 months.
Showing 26221–26240 of 29,188 recalls
Recalled Item: Crocodile (size 3) are two-armed Recalled by Snug Seat Inc Due to The bolts,...
The Issue: The bolts, which secure the handles, on the Crocodile (size 3) could break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...
The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating...
The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Mammo is a multi-modality Recalled by GE Healthcare It Due to There is...
The Issue: There is a potential safety issue with the 8.0.2 version software of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens...
The Issue: Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Title 2 Bone Screw Remover Instrument Recalled by Zimmer, Inc. Due to...
The Issue: Possibility of the weld to the quick-connect breaking when force is applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...
The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Titanium Prosthesis Recalled by Medtronic Xomed, Inc. Due to One...
The Issue: One lot of the product was assembled using the Cam Head version of the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Epilor Syringe BD Franklin Lakes Recalled by Becton Dickinson & Company...
The Issue: BD has received several reports indicating that the plunger of the 7 mL BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Spine Recalled by Ebi, Llc Due to Polaris Translation Screw Failures...
The Issue: Polaris Translation Screw Failures were recently reported to Biomet Spine....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timberline Anchored Lateral Variable Retractable Sleeve LITPCR8600-2101-07...
The Issue: The inner diameter of the Sleeve shaft is undersized, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anchored Lateral Retractable Drill Recalled by Biomet Spine, LLC Due to The...
The Issue: The outer diameter of the Drill shaft is oversized; thereby, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timberline Anchored Lateral Fixed Retractable Sleeve Model No. 8630-0205....
The Issue: The inner diameter of the Sleeve shaft is undersized, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicutt fully automated incision making device for bleeding time...
The Issue: ITC has determined that the blade in their Surgicutt with Blotting Paper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan plus Negative Urine Combo 4 Sold outside of US Recalled by Siemens...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Urine Combo 2 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Breakpoint Combo 7 Product Usage:...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan plus Negative Breakpoint Combo 4 Sold outside of US Recalled by...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.