Model Number LEAD1058-70B |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Skin Erosion (2075)
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Event Date 12/07/2019 |
Event Type
Injury
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Manufacturer Narrative
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The manufacturing records were reviewed and no issues were found related to the nature of the complaint.The device was removed but not returned.
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Event Description
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It was reported to nevro that the patient experienced skin erosion at the lead site.The device was removed and there have been no reports of further complications regarding this event.
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Search Alerts/Recalls
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