Philips Respironics recalls Aeris EVO ventilators (all software versions except 1.05.06.00) sold outside US due to potential sudden loss of ventilation when battery alarm triggers but unit has 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 Aeris EVO ventilators (except software version 1.05.06.00) sold outside the US. The device may lose ventilation suddenly if a battery low alarm sounds but the unit still has power, which could be dangerous for patients using it.
The ventilator may show a battery low or power loss alarm while still having sufficient power. This could cause sudden loss of ventilation, which is dangerous for patients who rely on the device to breathe.
Patients using the Aeris EVO ventilator for pediatric or adult care are most at risk. The recall applies to units sold outside the US with specific serial numbers and model numbers listed in the record.
Check for the model number VT2110X24B and serial numbers listed in the record. The recall applies to units sold outside the US with software versions other than 1.05.06.00.
Verify if your ventilator shows a battery low or power loss alarm while still having power.
Reach out to Philips Respironics for guidance on next steps if you have the recalled device.
Yes, if it has a model number VT2110X24B and a serial number listed in the record, and was sold outside the US with software versions other than 1.05.06.00.
Check if your device shows a battery low or power loss alarm while still having power. Contact Philips Respironics for further instructions.
The recall record does not specify a fix or remedy.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1499-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1499-2024 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.
