JWJClass 2
Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
FDA adverse event reports and recall history for prosthesis, wrist, 3 part metal-plastic-metal articulation, semi-constrained (product code JWJ), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 497
- Deaths
- 0
- Injuries
- 460
- Malfunctions
- 35
Reports per year
712
913
1114
715
4816
3717
3118
12719
3420
821
6522
2623
1824
825
4226
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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