Philips Recall
Patient Information

Philips Respironics Recall

Philips Respironics has recalled some positive airway pressure devices because of potential health risks from sound abatement foam. The FDA has now identified this as a Class I recall

The American Academy Of Sleep Medicine has a patient information website. The following link was created for FAQ on the recall.

• Philips PAP device recall: FAQs for patients – Sleep Education

Alternatively, there is an excellent youtube video.  See link below.

• How to Register Your Philips SRC Medical Device – YouTube