KTBS

Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall

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 ...
ABC12

FDA recalls some Philips CPAP, BiPAP machines

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 ...
Overdrive

CPAP recall leaves truck drivers with sleep apnea between a rock and a hard place

Electronics manufacturing giant Philips is recalling millions of CPAP and BiPAP devices due to an issue that could potentially pose a health risk to users of the machines. In the wake of the recall, ...
WSB-TV

Recall alert: 17M Philips CPAP, BiPAP masks recalled over ‘serious safety concern’

WASHINGTON — Medical equipment company Philips Respironics has recalled at least 17 million masks used with breathing devices designed to treat patients with sleep apnea and other respiratory ...
CBS News 8

Yes, the FDA recommends using replacement Philips CPAP devices

Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...
KAKE.com

Recall: Philips Respironics CPAP, BiPAP, and Ventilators

(KAKE/FDA) - Philips Respironics has voluntarily recalled certain ventilators, BiPAP, and CPAP machines due to potential health risks. The polyester-based polyurethane (PE-PUR) sound abatement foam, ...