HERE’S INVESTIGATIVE REPORTER PAUL VAN OSDOL. THE RECALL AFFECTED MILLIONS OF BREATHING MACHINES MADE BY PHILIPS, WHICH HAS OFFICES HERE IN BAKERY SQUARE AND IN MORRISVILLE. ON SATURDAY, DON SCHREIBER ...

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 ...

In the wake of a disastrous recall involving defective sound-dampening foam in several of its breathing machines, Philips Respironics announced Monday that it was suspending sales of its continuous ...

(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, ...

Magnets in the recalled masks, used in breathing machines for sleep apnea, can interfere with pacemakers and other lifesaving medical devices. Philips Respironics has voluntarily recalled more than 17 ...

In 2021, polyester-based polyurethane (PE-PUR) foam used in Philips Respironics ventilators, CPAP and BiPAP machines was found to degrade and cause serious health issues or death, leading to a mass ...

BOSTON (CBS) -- An I-Team investigation into a recall of Philips Respironics Continuous Positive Airway Pressure (CPAP) machines has many sleep apnea patients telling WBZ-TV they are now left with a ...

The manufacturer, Philips Respironics, said it would compensate users of CPAP machines and other flawed devices that were recalled after they blew bits of foam into consumers’ mouths and lungs. By ...

The U.S. Food and Drug Administration (FDA) is warning that Philips Respironics continuous positive airway pressure (CPAP) machines, which are used to treat obstructive sleep apnea, should be ...

In Rochester, N.Y., Diane Coleman has relied on a machine to help her stay alive, but she worries that it might be slowly undermining her health. Her ventilator was among millions of breathing devices ...