Model Number A219 |
Device Problems
Premature Discharge of Battery (1057); Incorrect, Inadequate or Imprecise Result or Readings (1535); Battery Problem (2885)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 04/10/2023 |
Event Type
Injury
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Event Description
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It was reported that this subcutaneous implantable cardioverter defibrillator (s-icd) recorded a battery depletion (bd) alert.The estimated longevity decreased not as expected, from 39% to 16%, within two months.A request was made to have data from this device analyzed.Data analysis confirmed the battery appeared to be depleting more quickly than expected.Device replacement was recommended.This device remains in service.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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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 this subcutaneous implantable cardioverter defibrillator (s-icd) recorded a battery depletion (bd) alert.The estimated longevity decreased not as expected, from 39% to 16%, within two months.A request was made to have data from this device analyzed.Data analysis confirmed the battery appeared to be depleting more quickly than expected.Device replacement was recommended.This device was replaced and is expected to be returned for analysis.No additional adverse patient effects were reported.
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Search Alerts/Recalls
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