PAIClass 3
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
FDA adverse event reports and recall history for mesh, surgical, non-synthetic, urogynecologic, for pelvic organ prolapse, transvaginally placed (product code PAI), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 160
- Deaths
- 1
- Injuries
- 158
- Malfunctions
- 1
Reports per year
112
2913
914
1015
10616
318
120
122
Source: FDA adverse event reports by year received, 2012–2022. 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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