NNXClass 1
Device, Incontinence, Urosheath Type, Non-Sterile
FDA adverse event reports and recall history for device, incontinence, urosheath type, non-sterile (product code NNX), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 909
- Deaths
- 0
- Injuries
- 169
- Malfunctions
- 740
Reports per year
112
114
115
1216
10917
14718
13119
18020
14821
11122
4423
1024
1425
Source: FDA adverse event reports by year received, 2012–2025. 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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