KWBClass 3
Prosthesis, Hip, Hemi-, Acetabular, Cemented, Metal
FDA adverse event reports and recall history for prosthesis, hip, hemi-, acetabular, cemented, metal (product code KWB), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 6,780
- Deaths
- 8
- Injuries
- 6,057
- Malfunctions
- 464
Reports per year
1,55909
75210
4211
10712
2713
3214
3115
416
217
618
519
920
421
522
424
Source: FDA adverse event reports by year received, 2009–2024. 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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