FXRClass 1
Holder, Camera, Surgical
FDA adverse event reports and recall history for holder, camera, surgical (product code FXR), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 131
- Deaths
- 0
- Injuries
- 30
- Malfunctions
- 100
Reports per year
110
419
1420
521
3722
4323
1724
425
626
Source: FDA adverse event reports by year received, 2010–2026. 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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