Medical Device Recall Information


Philips Respironics Sleep and Respiratory Care devices

Request in-office materials to help inform patients

In June 2021, after discovering a potential health risk related to a part in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).

We are committed to supporting clinicians through the complete remediation process and will provide a range of resources to help you better inform, instruct, and support your patients.

Thank you for your patience and continued trust.

Display packet includes:

  • 50 4 x 6 Postcards
  • 2 11 x 17 Posters with scannable QR code

Request your display packet

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