Philips Respironics recalls all Trilogy EV300 ventilators except software version 1.05.06.00 due to potential sudden loss of ventilation when battery or power alarms trigger while unit has sufficient power.
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 EV300 ventilators except those with software version 1.05.06.00. This recall is because the device may lose ventilation suddenly when battery or power alarms activate even though the unit still has power.
The ventilator may show battery or power alarms even when it still has sufficient power. This can cause a sudden loss of ventilation, which is dangerous for patients who rely on the device for breathing support.
Pediatric and adult patients using the Trilogy EV300 ventilator are affected. Those with the specific model numbers listed in the recall are most at risk.
Check the model numbers listed in the recall (e.g., BL2200X15B, BR2200X18B) or the unique device identifiers (UDI-DI) provided. The ventilator has software versions except 1.05.06.00.
Verify the software version on your ventilator; if it's not 1.05.06.00, it is affected.
Reach out to Philips Respironics for instructions on how to fix the issue or get a replacement.
The ventilator may show battery or power alarms even when it has sufficient power, which could cause sudden loss of ventilation. Do not use it until the issue is resolved.
All software versions except 1.05.06.00 are affected.
Check the model numbers listed in the recall (e.g., BL2200X15B, BR2200X18B) or the unique device identifiers (UDI-DI) provided.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1502-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1502-2024 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.
