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Model Number FGS-0313 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Chest Pain (1776)
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Event Date 09/13/2019 |
Event Type
malfunction
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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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According to the reporter, about 30 minutes after the placement of the capsule, the patient experienced severe chest pain.The physician attempted to cold snare to remove the capsule, but it did not work.
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Search Alerts/Recalls
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