Urgent: medical device recall
Philips Respironics: CPAP and Bi-Level PAP Devices
Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit philips.com/src-update or click the link below:
See if your Device is Effected:
Click the link below to check if your device is effected and to register your machine with Philips Respironics for replacement.
Philips will be contacting you to replace your device after you register.
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