QHPClass N
Vertebral Body Tethering System
FDA adverse event reports and recall history for vertebral body tethering system (product code QHP), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 275
- Deaths
- 1
- Injuries
- 252
- Malfunctions
- 22
Reports per year
3820
10221
2522
4423
4124
2225
326
Source: FDA adverse event reports by year received, 2020–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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