GAKClass 2
Suture, Absorbable
FDA adverse event reports and recall history for suture, absorbable (product code GAK), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 264
- Deaths
- 4
- Injuries
- 127
- Malfunctions
- 132
Reports per year
211
312
214
115
2316
117
718
2419
2220
1321
2022
3323
2924
2425
826
Source: FDA adverse event reports by year received, 2011–2026. 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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