Home › Device types › IMB
Cabinet, Moist Steam
FDA product code IMB · Class 2 · Physical Medicine
0
Registered devices
3
Adverse events
5
Recalls
5
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-06-22 | Sybaritic, Inc | A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D |
| 2007-06-22 | Sybaritic, Inc | A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D |
| 2007-06-22 | Sybaritic, Inc | A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D |
| 2007-06-22 | Sybaritic, Inc | A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D |
| 2007-05-15 | Sybaritic, Inc | Sybaritic conducted a recall on the Hydration Station 806 because of the potential for hot water to spurt through steam ports into unit and cause burns. Also |
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