Philips Respironics recalls Trilogy Evo ventilators with specific model numbers for safety software updates. Affected units require a software update to resolve identified safety issues.
Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.
Philips Respironics is recalling certain Trilogy Evo ventilators due to safety issues that require a software update to fix. This recall involves specific model numbers sold in various countries.
The ventilators have a software issue that requires a specific update to resolve safety concerns. The update addresses previously identified safety problems without causing immediate harm.
Users of Trilogy Evo ventilators with specific model numbers sold in Australia, Benelux, Brazil, Canada, Germany, Great Britain, India, Italy, Japan, Korea, Latin America, Nordic countries, and other regions are affected. Patients using these ventilators are most at risk.
Check the model number on your Trilogy Evo ventilator. Affected models include AU2110X15B (Australia), BL2110X15B (Benelux), BR2110X18B (Brazil), and others listed in the recall notice. Also check the serial numbers provided in the recall list.
Download and install the mandatory software update Version 1.05.10.00 from Philips Respironics to resolve the safety issues.
No, you can continue using your ventilator after installing the software update.
Affected models include AU2110X15B (Australia), BL2110X15B (Benelux), BR2110X18B (Brazil), and others listed in the recall notice.
Download and install the mandatory software update Version 1.05.10.00 from Philips Respironics to resolve the safety issues.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-2944-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-2944-2024 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.
