HSAClass 3
Prosthesis, Knee, Hemi-, Femoral
FDA adverse event reports and recall history for prosthesis, knee, hemi-, femoral (product code HSA), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 2,315
- Deaths
- 1
- Injuries
- 1,990
- Malfunctions
- 233
Reports per year
26906
19907
28808
31209
24310
4311
3112
3013
1314
1115
116
317
422
225
126
Source: FDA adverse event reports by year received, 2006–2026. 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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