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. 2,547 recalls have been distributed to Tennessee in the last 12 months.
Showing 21001–21020 of 29,188 recalls
Recalled Item: Freedom60 Precision Flow Rate Tubing Sets Recalled by Repro-Med Systems,...
The Issue: On 2/24/2016 during post sterilization inspection of part number F180...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient...
The Issue: Panorama Central Station including the work station View Station, View...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All instrumentation associated with the Prelude PF Resurfacing Knee System....
The Issue: Inadequate design control.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helios HL3T and HLT Track Mounted Dental Lights Product Usage: Recalled by...
The Issue: The firm received two customer complaints local Pelton & Crane distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....
The Issue: The center bolt of the sling bar, which connects the bar to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...
The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Triglyceride_2 Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics has confirmed the ADVIA Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments...
The Issue: Reports relating to unintended patient or operator burns or operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments...
The Issue: Reports relating to unintended patient or operator burns or operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Brilliance Workspace NM Nuclear medicine image display and...
The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Brilliance Workspace NM Special Nuclear medicine image display and...
The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal DX/HX/EX AutoSPECT Pro Software Application Recalled by...
The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.