EYJClass 1
Holder, Ureteral Catheter
FDA adverse event reports and recall history for holder, ureteral catheter (product code EYJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,176
- Deaths
- 0
- Injuries
- 59
- Malfunctions
- 1,114
Reports per year
110
213
314
215
216
11717
18218
15719
23420
17621
11822
9823
4324
2125
726
Source: FDA adverse event reports by year received, 2010–2026. 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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