Related manufacturer reference number: 2017865-2024-34941, related manufacturer reference number: 2017865-2024-34942, related manufacturer reference number: 2017865-2024-34944.It was reported that the patient presented with pocket erosion.It was also noted that the implantable cardioverter defibrillator migrated.The entire system was explanted.Further information was requested however, was not provided.
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The device was returned and analyzed in the lab.Interrogation of the device revealed the device was above elective replacement indicator (eri) upon receipt.Telemetry, pacing, sensing, impedance, hv output, hv shock, patient notifier were tested on the bench.No anomaly was detected.
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