JDJClass 2
Mesh, Surgical, Acetabular, Hip, Prosthesis
FDA adverse event reports and recall history for mesh, surgical, acetabular, hip, prosthesis (product code JDJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 236
- Deaths
- 0
- Injuries
- 216
- Malfunctions
- 19
Reports per year
611
1012
1813
1514
1215
516
217
1518
3419
1420
1421
822
124
225
226
Source: FDA adverse event reports by year received, 2011–2026. 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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