Product Alerts & Recalls
June 14, 2021
Philips issues recall notification to mitigate potential health risks related to the sound abatement foam component in certain sleep and respiratory care devices.
Philips has issued a global recall for several CPAP, Bi-level and Ventilator devices, including DreamStation and System One machines.
To view details on this recall please view the attached link which includes details of the affected machines, along with Philip’s advice to patients visit the Philips website for the latest updates.
mySleep® have not sold any of these affected machines.
This notification is issued as a public awareness announcement to ensure that any of our patients who may have previously purchased a device from another supplier.
Please feel free to contact us if you have any questions or concerns.