Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall
By Jen Christensen and Katherine Dillinger, CNN The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has determined a reasonable probability that a product could “cause serious adverse health consequences or death.”
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