MUMClass 2
Stent, Metallic, Expandable, Duodenal
FDA adverse event reports and recall history for stent, metallic, expandable, duodenal (product code MUM), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 988
- Deaths
- 55
- Injuries
- 428
- Malfunctions
- 502
Reports per year
7112
6213
4314
5115
4116
8517
4918
3519
3220
7021
2822
5323
3424
3225
426
Source: FDA adverse event reports by year received, 2012–2026. 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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