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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
11,149
Deaths
0
Injuries
1,998
Malfunctions
9,151

Reports per year

24
25
26

Source: FDA adverse event reports by year received, 20242026. Reporting paused twice in 2026 during FDA reporting-system changes 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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