FMRClass 1
Device, Transfer, Patient, Manual
FDA adverse event reports and recall history for device, transfer, patient, manual (product code FMR), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 126
- Deaths
- 2
- Injuries
- 36
- Malfunctions
- 82
Reports per year
112
813
414
415
616
217
818
1519
220
821
622
1023
1024
1025
1326
Source: FDA adverse event reports by year received, 2012–2026. 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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