MFI
Product code MFI
FDA adverse event reports and recall history for product code mfi (product code MFI), from the public MAUDE 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 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.
Monitor product code mfi automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.