Philips recalls OmniLab Advanced+ CPAP machines due to plastic parts causing VOC off-gassing. Affected units have specific serial numbers. Stop using immediately to avoid potential health risks.
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Philips is recalling certain OmniLab Advanced+ CPAP machines that may release harmful chemicals (VOCs) from their plastic components. This could pose a health risk, especially for people using the device nightly.
The motor assemblies in these devices use nonconforming plastic that can off-gas volatile organic compounds (VOCs). While VOCs are common in many products, this specific issue may cause health concerns for people using the device regularly.
Patients using the Philips OmniLab Advanced+ CPAP machines for sleep apnea treatment are most at risk. The recall affects specific units with listed serial numbers.
Check for the model number 1109581 and serial numbers listed in the recall notice. The affected units have specific serial numbers starting with L28664716B714 through L304097046ACC.
Look for the model number 1109581 on your device to confirm if it's affected.
Reach out to Philips Respironics for assistance with the recall process.
Philips recalls these CPAP machines because the motor assemblies use nonconforming plastic that can off-gas volatile organic compounds (VOCs).
Check for the model number 1109581 and serial numbers listed in the recall notice (starting with L28664716B714 through L304097046ACC).
Contact Philips Respironics directly for guidance on the recall process.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1657-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-1657-2022 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
