(Washington, D.C.) – The U.S. Food and Drug Administration (FDA) issued a safety communication to provide additional information about the voluntary recall of SoClean2 and SoClean3 equipment used to clean, sanitize or disinfect CPAP devices and accessories.
This SoClean device recall includes new instructions for device use, including the importance of using a hose and mask adapter provided by the company. This voluntary recall is intended to help reduce potential health risks of exposure to ozone gas after the use of SoClean2 or SoClean3 equipment.
