Royal Philips (NYSE:PHG) is no longer taking orders of sleep therapy systems as it handles a serious recall involving millions of the devices.
“As a consequence of the prioritization of the repair or replace actions, we are currently not taking new orders for sleep therapy systems while masks and other consumables, of course, continue to be sold,” CEO Frans van Houten said during a July 26 earnings call, transcribed by Seeking Alpha.
Van Houten said it will take 12 months after regulatory approval to address problems with all the devices, which have a polyester-based polyurethane (PE-PUR) sound abatement foam that could potentially break down and enter a device’s air pathway.
The FDA recently designated the recall as Class I, noting that users of the Philips ventilator devices face a host of health problems and toxic carcinogenic effects. The agency said that there have been more than 1,200 complaints and more than 100 injuries.
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