Model Number NEU_ENTERRA_INS |
Device Problem
Inappropriate/Inadequate Shock/Stimulation (1574)
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Patient Problem
Electric Shock (2554)
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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.- attachment: [mw5073402.Pdf].
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Event Description
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The healthcare provider (hcp) reported via the user facility that the device was replaced due to shocking.The patient outcome was hospitalization.The diagnosis for use was gastroparesis.There were no further complications reported as a result of this event.
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Search Alerts/Recalls
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