Chair, Examination And Treatment
FDA adverse event reports and recall history for chair, examination and treatment (product code FRK), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 652
- Deaths
- 1
- Injuries
- 36
- Malfunctions
- 584
Reports per year
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- Open, ClassifiedUnder Investigation by firm
Symmetry Plus Treatment Recliner - general hospital use as a convenient seating surface for patients or guests to sit, Model Number 3500, Part # 3500000710
Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
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