Imtmedical Ag
FDA adverse event reports naming Imtmedical Ag as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: IMTMEDICAL AG.
- Total reports
- 1,966
- Deaths
- 12
- Injuries
- 569
- Malfunctions
- 1,385
Reports per year
42419
24320
57221
37022
31623
4124
Source: FDA adverse event reports by year received, 2019–2024. 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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