Model Number LEAD3005-50B |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Spinal Cord Injury (2432)
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Event Date 03/11/2021 |
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's lead was impinging on the spinal cord.The device was removed and the patient recovered without sequelae.
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Event Description
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This report is to update the component code.
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Search Alerts/Recalls
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