Model Number L300 |
Device Problem
Premature Discharge of Battery (1057)
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Patient Problems
Dyspnea (1816); Edema (1820); No Consequences Or Impact To Patient (2199)
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Event Date 12/30/2019 |
Event Type
Injury
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Manufacturer Narrative
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As no further information concerning this report is expected, our investigation is complete.This investigation will be updated should further information be provided.
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Event Description
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It was reported that this pacemaker exhibited premature battery depletion (pbd).Additionally, the patient experienced shortness of breath due to edema.To date, the pacemaker remains in service.No adverse patient effects were reported.
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Manufacturer Narrative
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As no further information concerning this report is expected, our investigation is complete.This investigation will be updated should further information be provided.This supplemental report is being filed to correct as reported patient code.
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Event Description
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It was reported that this pacemaker exhibited premature battery depletion (pbd).Additionally, the patient experienced shortness of breath due to edema.To date, the pacemaker remains in service.No adverse patient effects were reported.Additional information obtained from the field which indicated that the device was explanted.No additional adverse patient effects were reported.
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Search Alerts/Recalls
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