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. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22261–22280 of 29,188 recalls
Recalled Item: Physio-Control QuikCombo Pacing/Defibrillation/ECG Electrodes RediPak¿...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediTrace Cadence Adult Zoll Recalled by Covidien LLC Due to Multi-Function...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System with software versions VB10B and lower...
The Issue: The ACUSON SC2000 ultrasound system considers uppercase/lowercase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid...
The Issue: Some devices exhibit backup VVI operation due to a backup reset.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...
The Issue: Cracks were discovered in the PET tray of a small population of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIVATORS HEMOCOR HPH700 Recalled by Medtronic Perfusion Systems Due to...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC PERFUSION TUBING PACKS (with potentially affected...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...
The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actifuse ABX/Actifuse MIS System A bone void filler intended only Recalled...
The Issue: Baxter Healthcare is issuing a voluntary recall for all lots of Actifuse ABX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software and firmware bugs
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....
The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...
The Issue: patient procedure interruption due to a potential system failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...
The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIRMap 60mm Catheter Recalled by Abbott Electrophysiology Due to The...
The Issue: The expiration date was incorrectly printed on the pouch/box labels of 19...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: The Centricity Universal Viewer...
The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LX3 Floor Stand for Endure Luxite Envision Optical System Recalled by Alcon...
The Issue: Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.