LYSClass 1
Bone Mill
FDA adverse event reports and recall history for bone mill (product code LYS), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,272
- Deaths
- 0
- Injuries
- 11
- Malfunctions
- 1,259
Reports per year
101
202
110
111
214
117
4618
5419
6620
17321
20122
38623
30524
2625
626
Source: FDA adverse event reports by year received, 2001–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2006-11-14TerminatedOther
Medtronic Sofamor Danek Bone fragmentor Ref Number/Model # 9150111
Metal bone fragmentor was causing metal shavings to be released into the resultant fragmented tissue during use.
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