EYAClass 1
Stylet, Ureteral
FDA adverse event reports and recall history for stylet, ureteral (product code EYA), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 205
- Deaths
- 0
- Injuries
- 57
- Malfunctions
- 146
Reports per year
197
198
100
202
717
1318
1119
820
3321
2122
2623
2724
2325
3126
Source: FDA adverse event reports by year received, 1997–2026. 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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