EXHClass 1
Bag, Urinary, Ileostomy
FDA adverse event reports and recall history for bag, urinary, ileostomy (product code EXH), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 539
- Deaths
- 0
- Injuries
- 80
- Malfunctions
- 459
Reports per year
109
210
413
8814
2715
916
11218
9319
8920
221
1022
2823
5924
1325
126
Source: FDA adverse event reports by year received, 2009–2026. 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.
Monitor bag, urinary, ileostomy automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.