MIRClass 3
Shunt, Portosystemic, Endoprosthesis
FDA adverse event reports and recall history for shunt, portosystemic, endoprosthesis (product code MIR), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 444
- Deaths
- 25
- Injuries
- 260
- Malfunctions
- 146
Reports per year
912
1113
814
615
816
1317
2018
2919
1420
1321
2322
2223
4024
1625
1526
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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