Skip to content

Senza® CHGR1000Recalls & reported problems

Nevro Corp. · Senza® Charger Kit · Class 3

All models of Senza (13)

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 00813426020121), received between May 22, 2017 and May 22, 2017 — 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

  • Tachycardia1

Recent adverse event reports

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

  • InjuryMay 22, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED TO NEVRO THAT A PATIENT EXPERIENCED A TINGLING SENSATION WHILE CHARGING THE IPG. THE SENSATION INTENSIFIED AND THE PATIENT REQUIRED ASSISTANCE TO END THE CHARGING SESSION. ADDITIONALLY HE EXPERIENCED SYMPTOMS OF TACHYCARDIA FOLLOWING THIS INCIDENT. THE THERAPY IS CURRENTLY OFF AND PATIENT IS UNDER THE CARE OF A CARDIOLOGIST.

    Patient problems: Tachycardia

    MAUDE report 6583576 ↗

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

All Stimulator, Spinal-Cord, Totally Implanted For Pain Relief devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page