Model Number NIPG1500 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Inflammation (1932); Muscle Weakness (1967)
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Event Date 03/29/2020 |
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 not removed.
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Event Description
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It was reported to nevro that the patient was hospitalized for inflammation and leg weakness.The patient was treated with injections and discharged.There have been no reports of further complications regarding this event.
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Event Description
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Follow-up indicated that the physician reviewed an mri and noted no abnormalities.The issue did not seem related to the device.
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Search Alerts/Recalls
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