HSHClass 2
Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)
FDA adverse event reports and recall history for prosthesis, knee, hemi-, tibial, resurfacing (uncemented) (product code HSH), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 8,110
- Deaths
- 7
- Injuries
- 6,536
- Malfunctions
- 1,075
Reports per year
22704
37205
49606
64807
87908
1,11509
54310
2211
7912
3713
1614
1815
317
318
122
Source: FDA adverse event reports by year received, 2004–2022. 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.
Monitor prosthesis, knee, hemi-, tibial, resurfacing (uncemented) automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.