IOYClass 1
Support, Arm
FDA adverse event reports and recall history for support, arm (product code IOY), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 173
- Deaths
- 0
- Injuries
- 11
- Malfunctions
- 159
Reports per year
510
111
912
1413
1414
315
1216
217
318
619
1620
2521
1322
2423
724
Source: FDA adverse event reports by year received, 2010–2024. 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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