Nevro Corp.
FDA adverse event reports naming Nevro Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: NEVRO CORP..
- Total reports
- 5,954
- Deaths
- 931
- Injuries
- 4,786
- Malfunctions
- 234
Reports per year
12117
41918
51719
42720
57921
61822
79323
1,17324
97625
33126
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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