![]() So without that CPAP machine, there’s a possibility that I could stop breathing while I’m sleeping and die." "I experience chronic obstructive sleep apnea, which means I stop breathing about 40 times an hour. Shawn was prescribed the Philips-brand DreamStation CPAP machine and said everything was working smoothly until a day recently when he called his doctor, looking for replacement parts for the machine. No one had told him about the recall, Shawn said, until he mentioned the CPAP machine he uses over the phone. "It really kind of upset me that nobody called, and I don’t know how many other people are unaware of this too," Shawn said. #Nonton wiro sableng 2018 indoxxi androidĭownload our local news and weather app for iOS or Android - and choose the alerts you want.īut now, she’s among up to four million people searching for answers and an alternative after Philips voluntarily recalled millions of its breathing devices in June due to serious safety concerns.Philips announced the recall of some of its most popular CPAP, BiPAP and ventilator devices on the market on June 14, 2021. The recall affected more than a dozen CPAP, BIPAP and mechanical ventilator machines after testing showed that sound abatement foam inside the devices can degrade into small particles that can be inhaled or swallowed. The company also found the foam could release harmful chemicals into the device’s airway. Though Philips states it has received a ‘limited number of reports of possible patient impact,” The Food and Drug Administration warns the problems can “result in serious injury, which can be life-threatening, cause permanent impairment, and require medical intervention to prevent permanent damage.” The FDA has labeled the action its most serious type of recall, Class I. Several Philips customers, like Domingo, told News4 they’re upset for a variety of reasons, including that they weren’t immediately notified of the recall and because Philips does not yet have a replacement for their damaged machines. The company is still waiting on regulatory approval to deploy repair and replacement kits now in production. Philips told News4 it launched a “comprehensive communication program” to notify patients worldwide, including through call centers and dedicated mailings, and is working with medical device retailers to directly reach out to clients.īut Domingo said she only heard about the recall through a coworker a month after it was announced, and faces a terrible choice. No, don't use it,’” Domingo said, adding, “This is life-altering.” Class Action Lawsuits Filed “My health care provider doesn't know what to say. The issue is now the subject of at least two class action lawsuits on behalf of affected customers. #Nonton wiro sableng 2018 indoxxi android. ![]()
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