MFJClass 2
Device, Endoscopic Suturing
FDA adverse event reports and recall history for device, endoscopic suturing (product code MFJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 843
- Deaths
- 1
- Injuries
- 167
- Malfunctions
- 638
Reports per year
4805
3206
5107
11208
11509
4010
2211
1112
413
514
1115
616
417
118
123
Source: FDA adverse event reports by year received, 2005–2023. 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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