Users of Philips-branded health machines that are subject to a recall have mere weeks to register their devices so they can get a repair or replacement.
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The affected devices are certain models of Philips' Continuous Positive Airway Pressure (CPAP) and Bi-level Positive Airway Pressure (Bi-Level PAP) machines.
These are commonly used to treat sleep apnoea and other health conditions that impair breathing, especially during sleep.
Both are subject to the recall, which was issued in July 2021. If left unfixed, the foam used in the blower box to reduce the machine's noise may break down into particles and release chemicals or gases which may be inhaled or ingested. Long term continued use of affected machines may lead to symptoms including headaches, nausea, inflammatory responses, asthma and possible carcinogenic effects.
Owners of such models can get their devices replaced or repaired, but must register their devices here to claim it. The registration process will close in early 2024.
The devices in question were all manufactured before April 26, 2021, and affects all device serial numbers.
To check the exact models affected, click here.
Most of the affected devices are in the first-generation DreamStation product family.
The Therapeutic Goods Administration has been monitoring the recall's progress.
For more information about the recall, phone 1800 009 579 or click here.
