Model Number G247 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Syncope/Fainting (4411)
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Event Date 11/12/2023 |
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 the patient with this cardiac resynchronization therapy defibrillator (crt-d) experienced a syncopal event, and the crt-d brought the patient back.The patient spent some days in the hospital and was contacted by the physician.The crt-d remains in service.No additional adverse patient effects were reported.
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Manufacturer Narrative
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H6: impact codes field updated.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 the patient with this cardiac resynchronization therapy defibrillator (crt-d) experienced a syncopal event, and the crt-d brought the patient back.The patient spent some days in the hospital and was contacted by the physician.The crt-d remains in service.No additional adverse patient effects were reported.
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Search Alerts/Recalls
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