Unomedical Um-d
FDA adverse event reports naming Unomedical Um-d as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: UNOMEDICAL UM-D.
- Total reports
- 11,165
- Deaths
- 0
- Injuries
- 2,025
- Malfunctions
- 9,140
Reports per year
323
57724
7,91425
2,67126
Source: FDA adverse event reports by year received, 2023–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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