Notice for Sleep Apnea Patients Using Philips Respironics CPAP/BiPAP Products


On June 14, 2021, Philips Respironics issued a voluntary keep in mind of its CPAP, BiPAP and mechanical ventilator gadgets. The remember is due to ability dangers associated with the froth used to reduce the sound and vibration of the motor. Those dangers include however aren’t limited to complications, nausea, infection of the eyes, nostril or pores and skin or capability most cancers brought about from toxic gases. Philips Respironics has recommended that you forestall using the recalled units and check together with your treating sleep professional to make an knowledgeable selection about whether or not the benefits of endured use outweigh the capacity risks.

What must sleep apnea sufferers do in reaction to this alert?
At this time, SSM Health recommends which you reach out in your company so collectively you may make an informed decision about whether the benefits of persisted use outweigh the ability bipap machine risks diagnosed within the take into account observe.

How can I analyze whether my tool has been recalled?
Philips Respironics created an online registration system to allow patients to look up their tool serial number and start a declare if their unit is affected by the consider. You should check in any affected tool through the internet site, Philips.Com/src-update, or by using telephone at 1-877-907-7508.

Where do I discover my tool’s serial variety?
The serial range is on the lowest of your tool. See the picture.

Turn your system over
The serial number is positioned at the left of the machine and could begin with a J, P, or C
Please do now not use the number at the right aspect that begins with H – this is for the humidifier
Where to discover the serial number on your CPAP tool
When can I update my recalled tool?
Philips Respironics plans to deal with the remediation of the recalled products. The agency indicates that it’s going to update the contemporary insulation foam with new cloth as quick as feasible and has already began arrangements. We do now not but recognise the time-frame for tool substitute. They are nevertheless running through the development and timing of that program and plan to send a letter to the owners of the recalled gadgets at an undetermined future date. In addition, the enterprise is recommending that customers and patients halt use of ozone-related cleansing products and cling to their tool commands for authorized cleansing strategies.

How do I replace my recalled tool?
If you’ve got acquired your substitute PAP tool from Respironics you may find this video’s commands beneficial. If you’ve got any issues or questions with getting your new device installation, you may call Respironics at 833-262-1871.


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