MSFClass 2
Hemodialyzer, Re-Use, High Flux
FDA adverse event reports and recall history for hemodialyzer, re-use, high flux (product code MSF), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,219
- Deaths
- 3
- Injuries
- 23
- Malfunctions
- 1,164
Reports per year
199
102
204
2206
50907
65908
510
1611
113
114
115
123
Source: FDA adverse event reports by year received, 1999–2023. 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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