Philips recalls Trilogy 200 Ventilators with specific model numbers due to potential separation of silicone sound abatement foam, which could block air intake and reduce therapy effectiveness.
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 is recalling certain Trilogy 200 Ventilators because a replacement silicone foam might detach from the device. If it separates, it could block air intake, reducing therapy effectiveness or causing the device to alarm.
The replacement silicone sound abatement foam installed in some Trilogy 200 devices can separate from the plastic backing. If it detaches, it may block air intake, reducing the delivered therapy volume or pressure and causing the device to alarm.
Users of the recalled Trilogy 200 Ventilators with specific model numbers listed in the recall. Patients relying on these devices for respiratory therapy are most at risk.
Check the model numbers listed in the recall: 1040005, U1040005, 1040005B, U1040005B, CA1032800B, CA1032800, KO1032800, and other specific model numbers provided in the recall notice.
Verify your device's model number against the list provided in the recall notice to confirm if it is affected.
Reach out to Philips Respironics customer support for further assistance or to confirm if your device needs replacement.
The replacement silicone sound abatement foam installed in some Trilogy 200 devices may separate from the plastic backing, potentially blocking air intake and reducing therapy effectiveness.
The affected model numbers include 1040005, U1040005, 1040005B, U1040005B, CA1032800B, CA1032800, KO1032800, and other specific model numbers listed in the recall notice.
No, the recall does not require immediate discontinuation of use. However, you should check if your device is affected and contact Philips for guidance.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0883-2023 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0883-2023 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.
