Model Number V173 |
Device Problem
Incorrect, Inadequate or Imprecise Result or Readings (1535)
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Patient Problems
Fatigue (1849); Device Overstimulation of Tissue (1991); Malaise (2359)
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Event Date 11/10/2020 |
Event Type
Injury
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Manufacturer Narrative
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The product has been received for analysis.This report will be updated upon completion of analysis.
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Event Description
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It was reported that this cardiac resynchronization therapy pacemaker (crt-p) had entered safety mode.The patient was not feeling well, and felt a phrenic nerve stimulation from unipolar pacing.The patient noted feeling shortness of breath when walking up a small incline.Technical services (ts) advised the health care professional (hcp) to replace the device and send it back for analysis.This cardiac resynchronization therapy pacemaker (crt-p) was explanted.No additional adverse patient effects were reported.
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Manufacturer Narrative
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The product has been received for analysis.This report will be updated upon completion of analysis.Upon receipt at our post market quality assurance laboratory, this device was thoroughly inspected and analyzed.Interrogation of the device confirmed it was operating in safety mode due to system resets.It was confirmed that brady therapy remained available.The system resets caused the device to enter safety mode.Engineers determined that this device was demonstrating behavior consistent with a high internal cell impedance within the battery.The high internal impedance resulted in the system resets due to temporary high-power consumption related to telemetry attempts and subsequent reversion to safety mode operation.Boston scientific has issued a field safety notice regarding ingenio extended life (el) and cardiac resynchronization therapy pacemaker (crt-p) devices that may exhibit this behavior.This particular device is included in the high impedance in ingenio extended life (el) pacemaker and crt-p advisory population.
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Event Description
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It was reported that this cardiac resynchronization therapy pacemaker (crt-p) had entered safety mode.The patient was not feeling well, and felt a phrenic nerve stimulation from unipolar pacing.The patient noted feeling shortness of breath when walking up a small incline.Technical services (ts) advised the health care professional (hcp) to replace the device and send it back for analysis.This cardiac resynchronization therapy pacemaker (crt-p) was explanted and returned.No additional adverse patient effects were reported.
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Search Alerts/Recalls
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