NUNClass 2
Bone Grafting Material, Human Source
FDA adverse event reports and recall history for bone grafting material, human source (product code NUN), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 121
- Deaths
- 0
- Injuries
- 88
- Malfunctions
- 19
Reports per year
1311
1512
2513
214
615
116
1017
418
1019
620
621
322
224
625
326
Source: FDA adverse event reports by year received, 2011–2026. 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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