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.

FDA: http://ht.ly/hMkQ30rL0GE

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/philips-issues-recall-notification-mitigate-potential-health-risks-related-sound-abatement-foam

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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