Penn Live

FDA says Philips Respironics notification of CPAP, BiPAP recall has been ‘inadequate’

In June of 2021, Philips Respironics issued a recall for some of its CPAP and BiPAP machines. Now the U.S. Food and Drug Administration says the notification to users about the recall “have been ...
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, ...
Penn Live

Philips Respironics recalls CPAP, BiPAP masks because magnets can affect other medical devices

Philips Respironics has recalled some face masks used with CPAP and BiPap machines because they have magnetic headgear clips that can interfere with other medical devices. The recalled masks are the ...
NBC Chicago

FDA Finds Maker of Recalled Sleep Aid Devices Knew Of Problems For Years, But Didn't Act

Millions of people across the country were jostled awake this year over fearful news: A critical device they were prescribed and relied on each night for sleep was suddenly labeled a hazard to their ...
International Business Times

Philips Respiratory Machine Recall 2022: Plastic Contamination Prompts Another Recall Of ...

A custom-made valve fits to the top of full-face masks, where the snorkel is meant to go, allowing them to connect to standard BiPAP machines that feed pressurised air into masks AFP / Kenzo ...
Reuters

Respironics says FDA gives marketing approval to BiPAP autoSV

March 7 (Reuters) - Respironics Inc. said U.S. regulators granted approval to market its ventilatory support device, BiPAP autoSV, for sleep-disordered breathing patients. The company said the device ...