FROM SHADYSIDE TONIGHT. PHILIPS REIS RUN ROAD RECALLED MILLIONS OF CPAPS BIPAPS AND VENTILATORS AFTER THE FDA SAID FOAM INSULATION INSIDE THOSE MACHINES WAS A HEALTH RISK. BUT IN A LAWSUIT, PHILIPS ...
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 ...
AND HAS THE NEW INFORMATION TONIGHT. THE OWNERS OF PHILIPS RESPIRONICS, CPAP AND OTHER BREATHING MACHINES ARE RECEIVING THIS NOTICE IN THE MAIL OF A PROPOSED CLASS ACTION SETTLEMENT. EIGHT ON YOUR ...
An online reviewer is warning about a CPAP machine recall. He claims The Philips Dreamstation CPAP device, recalled in 2023, is still being used and could pose a cancer risk to users. Featured Video ...
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 ...
People who have bought, leased or rented certain Philips Respironics sleep apnea machines can now file a claim for restitution. The Dutch medical equipment maker recently agreed to pay at least $479 ...
This article originally appeared in ProPublica. ProPublica is a Pulitzer Prize-winning investigative newsroom. Sign up for The Big Story newsletter to receive stories like this one in your inbox. For ...
Three years after one of the largest medical device recalls in history, the fallout – health-wise and financial – continues to impact many patients with sleep apnea. Now a critical deadline is ...
If you use a Philips CPAP machine, you have another thing to keep you awake at night: The FDA issued a warning Tuesday to patients and health care providers saying the company’s DreamStation 2 ...
Medical device company Philips reached a settlement Monday to shell out $1.1 billion to cover hundreds of personal injury lawsuits linked to its respiration and sleep apnea machines. The manufacturer ...
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 ...
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