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. 2,666 recalls have been distributed to Tennessee in the last 12 months.
Showing 9581–9600 of 29,188 recalls
Recalled Item: 728327 Ingenuity CT Upgrades-Computed Tomography X-ray system Recalled by...
The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance...
The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 728321/728323 CT5000 Ingenuity Plus/Pro/Premium-Computed Tomography...
The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation (Radiation Treatment Planning System) : RayStation 9A Recalled by...
The Issue: Initial delivery positions will be set incorrectly when having setup beam(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 /...
The Issue: Due to real-time stability study failures resulting in increase rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel plus (Pneumoplus) Part Numbers: Part No:...
The Issue: Due to real-time stability study failures resulting in increase rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: reSET-O Mobile App Recalled by Pear Therapeutics, Inc. Due to Due to a...
The Issue: Due to a software issue, patients with a urine drug screen (UDS) received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: reSET Mobile App Recalled by Pear Therapeutics, Inc. Due to Due to a...
The Issue: Due to a software issue, patients with a urine drug screen (UDS) received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simpleware ScanIP software. For transfer of imaging information from a...
The Issue: A issue (bug) has been identified with the interface and image software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simpleware ScanIP medical software. For transfer of imaging information from...
The Issue: A issue (bug) has been identified with the interface and image software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recirculator 8.0s Disposable Lavage Kit (product code number 8100) Recalled...
The Issue: The patient may be exposed to potential aluminum ion release during warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Driveline Extension Cable Recalled by Heartware, Inc. Due to...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus Stapler-intended for transection Recalled by...
The Issue: Mislabeled: Labeled on the package as 60mm contains 45mm devices
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Outflow Graft Recalled by Heartware, Inc. Due to Medtronic is...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Accessories Recalled by Heartware, Inc. Due to Medtronic...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Driveline Extension Cable Recalled by Heartware, Inc. Due to...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...
The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.