Model Number NEU_ENTERRA_INS |
Device Problem
Device Operates Differently Than Expected (2913)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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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.See [mw5073409.].
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Event Description
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The healthcare provider (hcp) reported via the user facility that a revision was performed due to dysfunction of the device.This event occurred (b)(6) 2017.The patient outcome was hospitalization.There were no further complications reported as a result of this event.
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Search Alerts/Recalls
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