Micrus Endovascular, LLC
FDA adverse event reports naming Micrus Endovascular, LLC as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MICRUS ENDOVASCULAR, LLC.
- Total reports
- 1,326
- Deaths
- 22
- Injuries
- 278
- Malfunctions
- 1,021
Reports per year
32612
28213
71814
Source: FDA adverse event reports by year received, 2012–2014. 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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