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Philips Recalls Millions of Ventilators and CPAP Machines Over Toxic Foam Fears; Replacement Delays Leave Users Concerned

  • Philips Respironics recalled millions of ventilators, CPAP and BiPAP machines due to potentially toxic foam breaking down and releasing chemicals. The FDA categorized it as a Class 1 recall, its most serious type.

  • The recalled machines were sold globally. Affected models include DreamStations and other Philips Respironics devices. Users should check if their device's model and serial number matches recalled ones.

  • The FDA warned the foam breakdown could cause headaches, asthma, cancer and other health issues. Philips initially agreed but now claims new testing shows low risk. Experts remain concerned.

  • To get a replacement, users must register affected devices on Philips' website and provide a doctor's prescription. Many users report delays in getting new machines.

  • Patients can report injuries/deaths to the FDA's MAUDE database. Social media has advice but experts say doctors are the best source.

propublica.org
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