Medtronic Inc. Cardiac Rhythm Disease Management recalls

5 recalls on record · latest: September 15, 2015

Official U.S. recall history for Medtronic Inc. Cardiac Rhythm Disease Management, compiled from official government records.

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Medtronic Inc. Cardiac Rhythm Disease Management recalls Medtronic Medical Device Identification Card for SureScan pacemaker patients. The front of this card identifies the imp…

September 15, 2015 · Medical device recalls Moderate risk Some Medical Device Identification Cards provided to SureScan pacemaker patient…

Medtronic Inc. Cardiac Rhythm Disease Management recalls Medtronic CryoConsole, models 106A3, 106E2, and 106A2-K For use in performing cardiac ablation procedures.

September 1, 2015 · Medical device recalls Moderate risk An issue with a USB memory component contained within a subset of CryoConsoles…

Medtronic Inc. Cardiac Rhythm Disease Management recalls Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, B…

March 23, 2015 · Medical device recalls Moderate risk Medtronic is conducting a voluntary recall of all former Covidien Trellis 6 and…

Medtronic Inc. Cardiac Rhythm Disease Management recalls Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…

March 17, 2015 · Medical device recalls Moderate risk Possible performance issue when used with specific AA-sized (LR6) batteries. Th…

Medtronic Inc. Cardiac Rhythm Disease Management recalls Medtronic, 10 Fr FlexCath Select Steerable Sheath 990065. The FlexCath Select Steerable Sheath (10 Fr Select) is used f…

February 23, 2015 · Medical device recalls High risk Clinicians observed debris, appearing to originate from the hemostasis valve on…