ILMClass 2
Bath, Sitz, Powered
FDA adverse event reports and recall history for bath, sitz, powered (product code ILM), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 162
- Deaths
- 1
- Injuries
- 36
- Malfunctions
- 121
Reports per year
194
4713
6114
1415
2016
617
218
619
520
Source: FDA adverse event reports by year received, 1994–2020. 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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