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Nevro® LEAD3005-90BRecalls & reported problems

Nevro Corp. · Surgical Lead Kit, 90cm · Class 3 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813426020428), received between Jun 7, 2018 and Jun 7, 2018 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Neurological Deficit/Dysfunction1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 7, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED TO NEVRO THAT SHORTLY AFTER THE IMPLANT PROCEDURE THE PATIENT DEVELOPED LEG PAIN AND LOSS OF SENSATION. SUBSEQUENTLY, THE PHYSICIAN EXPLANTED THE LEAD. THE IPG WAS LEFT IN PLACE FOR FUTURE RE-IMPLANT OF A NEW LEAD. THE PATIENT IS RECOVERING FROM HIS SYMPTOMS.

    Patient problems: Neurological Deficit/Dysfunction

    MAUDE report 7578134 ↗

Other Stimulator, Spinal-Cord, Totally Implanted For Pain Relief devices

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Sources and updates

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