KWFClass 2
Prosthesis, Finger, Polymer
FDA adverse event reports and recall history for prosthesis, finger, polymer (product code KWF), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 222
- Deaths
- 0
- Injuries
- 108
- Malfunctions
- 10
Reports per year
110
311
212
113
314
216
2318
519
220
221
522
623
124
325
226
Source: FDA adverse event reports by year received, 2010–2026. 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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