HWMClass 1
Osteotome
FDA adverse event reports and recall history for osteotome (product code HWM), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 712
- Deaths
- 0
- Injuries
- 29
- Malfunctions
- 678
Reports per year
512
1513
514
1015
716
4617
5818
5419
5720
7321
7522
7223
9324
5425
4426
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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