PAGClass 2
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator
FDA adverse event reports and recall history for mesh, surgical, non-synthetic, urogynecologic, for stress urinary incontinence, retropubic or transobturator (product code PAG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 756
- Deaths
- 0
- Injuries
- 752
- Malfunctions
- 2
Reports per year
108
8413
25614
7315
29916
1117
418
1719
420
521
122
123
Source: FDA adverse event reports by year received, 2008–2023. 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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