OTPClass 3
Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
FDA adverse event reports and recall history for mesh, surgical, synthetic, urogynecologic, for pelvic organ prolapse, transvaginally placed (product code OTP), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 11,652
- Deaths
- 256
- Injuries
- 10,902
- Malfunctions
- 483
Reports per year
49412
7,15013
77814
68415
41616
27017
39218
36819
17520
64721
11422
5923
3524
2825
326
Source: FDA adverse event reports by year received, 2012–2026. 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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