Philips recalls OmniLab Advanced + with Heated Tube Humidifier (Rx Only) due to potential VOC off-gassing from nonconforming plastic. Affected units have specific UDI-DI and model numbers. Consumers should contact Philips for details.
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Philips is recalling its OmniLab Advanced + with Heated Tube Humidifier (Rx Only) because plastic components may off-gas VOCs. This could pose a risk to health, especially for people with respiratory conditions, though the recall does not specify serious injury risks.
The humidifier's motor assemblies use nonconforming plastic that releases volatile organic compounds (VOCs) when in use. VOCs can irritate the respiratory system and may cause health issues for sensitive individuals, especially those with pre-existing respiratory conditions.
Patients using this humidifier for noninvasive ventilation support, particularly those with obstructive sleep apnea or respiratory issues. The risk is higher for individuals sensitive to VOCs.
Check for UDI-DI numbers 606959067837, 606959068001 or model numbers 1111124, R1111124. The serial numbers listed are L29084645477C, L303986771E8D, L303987043BC2, L3039871356A5, L30398768A57E, L303987892EE7, L30398795FD53, L30398849CD80.
Verify your unit's UDI-DI number (606959067837 or 606959068001) or model number (1111124 or R1111124).
Reach out to Philips Respironics for specific instructions on whether your unit is affected and next steps.
This recall applies only to medical devices prescribed for noninvasive ventilation support, specifically for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
The plastic components may off-gas VOCs, which could irritate the respiratory system, especially for individuals with sensitive respiratory conditions.
Check for UDI-DI numbers 606959067837 or 606959068001, or model numbers 1111124 or R1111124. The listed serial numbers are also affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1659-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-1659-2022 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.
