Model Number NIPG2500 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Seroma (2069)
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Event Date 01/15/2021 |
Event Type
Injury
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Manufacturer Narrative
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The manufacturing records were reviewed and no relevant nonconformities were found.The device was not returned.
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Event Description
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It was reported to nevro that the patient acquired a seroma.The patient was hospitalized and given antibiotics.The physician did not believe the seroma to be related to the device.The device was removed and there have been no reports of further complications regarding this event.
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Manufacturer Narrative
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This report is to update sections explant date and adverse event problem.For section describe event or problem.There was no physician assessment available regarding the seroma.
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Event Description
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This is a correction report.
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Search Alerts/Recalls
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