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/AEMS 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 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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