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PITTSBURGH – Citing diversity of citizenship and the amount in contested damages, Philips has removed a lawsuit centered on the death of a man using a recalled medical device to treat his sleep apnea, to federal court.
PITTSBURGH – A Louisiana woman alleges that her late husband died as a result of a device the defendants manufactured and sold to treat sleep apnea, without being informed until after his passing that the device in question had been subject to a widespread recall.
And some of the remediated breathing devices may not provide any treatment at all, FDA warns
There are 1,088 devices recalled in the U.S., the FDA said
Philips is recalling certain reworked DreamStation CPAP and BiPAP machines as they may deliver inaccurate or insufficient therapy.