Philips Respironics recalls Trilogy Evo O2 ventilators (all software versions except 1.05.06.00) due to potential sudden loss of ventilation when battery alarm triggers but power is still sufficient. Affected units have specific model numbers and serials listed in the recall.
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Philips Respironics is recalling all Trilogy Evo O2 ventilators except software version 1.05.06.00. The device may lose ventilation unexpectedly if the battery alarm sounds but the unit still has power. This could be dangerous for patients using the ventilator.
The ventilator may show a battery depleted or power loss alarm while still having sufficient power. This can cause sudden loss of ventilation, which is critical for patients relying on the device to breathe.
Patients using the Trilogy Evo O2 ventilator for pediatric or adult care are most at risk. Owners of the recalled units with specific model numbers and serials listed in the recall are affected.
Check if your unit has model numbers EE2100X15B, FR2100X14B, DE2100X13B, ES2100X15B, IA2100X15B, IT2100X21B, or ND2100X15B. Also check the serial numbers listed in the recall details.
Verify if your ventilator shows a battery depleted or power loss alarm while still having power. If so, stop using it immediately.
Reach out to Philips Respironics for guidance on next steps if you have a recalled unit.
No, this recall applies to all Trilogy Evo O2 ventilators except software version 1.05.06.00.
Check your model and serial numbers against the list provided in the recall. Contact Philips Respironics for specific instructions.
The recall does not specify a fix or safe usage condition; affected units should be checked with the manufacturer.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1503-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1503-2024 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.
