PAJClass 2
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
FDA adverse event reports and recall history for mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed (product code PAJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 787
- Deaths
- 1
- Injuries
- 782
- Malfunctions
- 4
Reports per year
6113
6614
28615
26716
9617
918
219
Source: FDA adverse event reports by year received, 2013–2019. 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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