MOUClass 3
Intravascular Radiation Delivery System
FDA adverse event reports and recall history for intravascular radiation delivery system (product code MOU), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 143
- Deaths
- 3
- Injuries
- 7
- Malfunctions
- 92
Reports per year
100
2601
4902
3603
1804
305
206
108
213
114
115
119
221
Source: FDA adverse event reports by year received, 2000–2021. 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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