OXFClass 2
Mesh, Surgical, Absorbable, Plastic And Reconstructive Surgery
FDA adverse event reports and recall history for mesh, surgical, absorbable, plastic and reconstructive surgery (product code OXF), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 343
- Deaths
- 0
- Injuries
- 342
- Malfunctions
- 1
Reports per year
1413
12914
10715
5216
2517
418
119
120
721
122
123
126
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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