HTGClass 2
Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
FDA adverse event reports and recall history for prosthesis, knee, hemi-, patellar resurfacing, uncemented (product code HTG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 2,066
- Deaths
- 2
- Injuries
- 1,886
- Malfunctions
- 102
Reports per year
3102
3703
3204
6905
10406
8007
17108
15309
14710
12311
5412
3913
1314
615
518
Source: FDA adverse event reports by year received, 2002–2018. 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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