OWTClass 2
Mesh, Surgical, Absorbable, Abdominal Hernia
FDA adverse event reports and recall history for mesh, surgical, absorbable, abdominal hernia (product code OWT), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 581
- Deaths
- 7
- Injuries
- 517
- Malfunctions
- 56
Reports per year
114
115
316
717
3118
6119
4520
5821
10422
7723
6524
8425
4426
Source: FDA adverse event reports by year received, 2014–2026. 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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