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 ...
Medscape

Philips Respironics Updates Device Use Correction

Philips Respironics has updated use instructions for three bi-level positive airway pressure machines, according to a recall statement posted by the US FDA. The recall does not include removal of the ...
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 ...
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 ...
Yahoo Finance

Philips provides update on completed set of test results for CPAP/BiPAP sleep therapy devices

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG; AEX: PHIA), today provides an update on the comprehensive test and research program of its subsidiary Philips Respironics to assess potential ...