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 26741–26760 of 29,188 recalls
Recalled Item: Mesa EZtest BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for use in...
The Issue: Mesa EZTest , Self-contained steam biological indicator, are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respironics V60 Ventilator Recalled by Respironics California Inc Due to...
The Issue: Respironics California, Inc. has initiated a recall on the V60 ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Deltran Disposable Pressure Transducer Kit (DPT Kit) Extracorporeal...
The Issue: Utah Medical Products, Inc. is recalling certain Deltran Disposable Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mesa Smart-Read EZTEST BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for...
The Issue: Self-contained steam biological indicator, are recalled because Mesa...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExactaMix 1200 and 2400 Compounders. Used as an automated pumping Recalled...
The Issue: Baxter Healthcare is recalling certain ExactaMix automated compounding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Power Wheelchair Recalled by Invacare Corporation Due to Unintended...
The Issue: Unintended slowing or deceleration, and on rare occasion, unanticipated and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Cardiovascular Custom Cardiovascular Procedure Kits containing an...
The Issue: Over-Pressure Safety Valves not cleared with an indication for use on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic INDURA 1P Intrathecal Catheter Recalled by Medtronic...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU5800 Clinical Chemistry Analyzer with Automation Ready Connection (All...
The Issue: The recall was initiated because Beckman Coulter has identified a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Sutureless Pump Connector Revision Kit Recalled by Medtronic...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intrathecal Catheter Pump Segment Revision Kit Recalled by...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed EL Programmable pumps Recalled by Medtronic...
The Issue: Medtronic is providing Healthcare Professionals with important safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic is providing Healthcare Professionals with important safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intrathecal Catheter Recalled by Medtronic Neuromodulation Due to...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMC Saddle Product Usage: The Ascension CMC is intended to Recalled by...
The Issue: As a result of a quality review, labelling content discrepancies were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX Evolution System Recalled by Carestream Health Inc. Due to...
The Issue: Due to potential for an x-ray exposure technique change.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler Set Single Conn./Ext DL Product Number: 050-87216...
The Issue: Cassette may leak during set up or during peritoneal dialysis treatment
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Vector Distractor Pin Holding Clamp Recalled by Synthes USA HQ, Inc....
The Issue: Synthes is initiating a voluntary Medical Device removal for specified part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX Instrument Recalled by Becton Dickinson & Co. Due to Electrical power...
The Issue: Electrical power module installed on some in vitro diagnostic instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Recalled by...
The Issue: The firm is initiating a Field Safety Correction for the labeling of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.