Model Number G138 |
Device Problems
Premature Discharge of Battery (1057); Battery Problem (2885)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/26/2024 |
Event Type
Injury
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that a request was made to have data from this cardiac resynchronization therapy defibrillator (crt-d) device analyzed.Data analysis confirmed that the power consumption is increasing in a gradual fashion.Device replacement was recommended.No adverse patient effects were reported.
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that a request was made to have data from this cardiac resynchronization therapy defibrillator (crt-d) device analyzed.Data analysis confirmed that the power consumption is increasing in a gradual fashion.Device replacement was recommended.No adverse patient effects were reported.Additional information received indicated that this crt-d device was explanted due to premature battery depletion (pbd).This device was replaced.No additional adverse patient effects were reported.
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Search Alerts/Recalls
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