Philips PAP, CPAP & Mechanical Ventilator Recall [US]

Philips Bi-Level PAP, CPAP & Ventilator Recall [US]

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US FlagUS/Silver Spring: Royal Philips, an Amsterdam, Netherlands establishment, recalls certain batch/lots of various Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (“CPAP”) and other Mechanical Ventilator Devices from the American marketplace to address identified potential health risks related to the Polyester-based Polyurethane (“PE-PUR”) Sound Abatement Foam component in these devices, a serious health and safety hazard requiring medical intervention.


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Additional information:
The US Food and Drug Administration (“FDA”) reports the following Bi-Level PAP, CPAP and Ventilators are subject to this recall:

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