MFI
Product code MFI
FDA adverse event reports and recall history for product code mfi (product code MFI), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 172
- Deaths
- 16
- Injuries
- 30
- Malfunctions
- 6
Reports per year
197
200
201
102
1503
3204
2805
3606
2607
2008
709
211
Source: FDA adverse event reports by year received, 1997–2011. 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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