Model Number LEAD3005-70B |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Muscle Weakness (1967); Numbness (2415); Spinal Cord Injury (2432)
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Event Date 06/01/2021 |
Event Type
Injury
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Manufacturer Narrative
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The manufacturing records were reviewed and no issues were found.The device was not available for return.
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Event Description
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It was reported to nevro that the device was removed after patient experienced weakness and numbness in the leg and difficulty walking.The patient is now recovering and is regaining mobility.
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Search Alerts/Recalls
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