Philips Respironics recalls certain Trilogy 100 Ventilators where replacement silicone sound abatement foam may separate from plastic backing, potentially reducing therapy volume or causing alarms. Affected models include 1054260, 1054096, U1054260, and others. No immediate action needed but check your device.
The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air inlet, which could result in a reduction in delivered therapy volume or pressure and could cause the device to alarm.
Philips Respironics is recalling certain Trilogy 100 Ventilators where replacement silicone sound abatement foam may separate from the plastic backing. If this happens, the foam could block air intake, reducing therapy volume or causing the device to alarm. This is a low-risk issue that doesn't require immediate action but should be checked.
The replacement silicone sound abatement foam installed in some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing. If this separation occurs, the foam could block air intake, reducing delivered therapy volume or pressure and causing the device to alarm.
Patients using the recalled Trilogy 100 Ventilators with specific model numbers (e.g., 1054260, 1054096) are most at risk. The issue is unlikely to cause serious injury but could affect therapy effectiveness.
Check your device for model numbers including 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, or other listed serial numbers. The recall covers specific models sold with these identifiers.
Identify your device model number by checking the label on the device or its packaging. Compare it to the list of affected model numbers provided in the recall.
The replacement silicone sound abatement foam installed in some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing, potentially blocking air intake and reducing therapy volume or causing alarms.
No immediate action is needed. The recall is low-risk and does not require stopping use, but you should check your device model to see if it's affected.
If your device is affected, contact Philips Respironics for further instructions. They may provide guidance on how to address the issue without needing to replace the device.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0882-2023 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0882-2023 from Philips Respironics. 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.
