Model Number NIPG1500 |
Device Problems
Adverse Event Without Identified Device or Use Problem (2993); Insufficient Information (3190)
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Patient Problems
Complaint, Ill-Defined (2331); Insufficient Information (4580)
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Event Date 12/10/2020 |
Event Type
Injury
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Manufacturer Narrative
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Analysis of the device is currently in progress.
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Event Description
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It was reported to nevro that the patient's device was removed.Nevro attempted to obtain additional information regarding the reason for the device removal but was unsuccessful.There were no reports of device-related issues from the patient prior to the incident.
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Manufacturer Narrative
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The device was returned and analyzed.Visual inspection of the returned device did not find any anomaly.Functional testing was performed and the device operated to specifications.Review of the patient's diagnostic data also showed no evidence of a device malfunction.The manufacturing records were reviewed and no non-conformities were found.
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Event Description
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The device was returned and analyzed.
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Search Alerts/Recalls
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