HOCClass 1
Clip, Iris Retractor
FDA adverse event reports and recall history for clip, iris retractor (product code HOC), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 289
- Deaths
- 0
- Injuries
- 57
- Malfunctions
- 221
Reports per year
411
112
1013
3114
2015
316
517
1118
419
420
622
923
924
7725
9026
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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