Philips Respironics recalls Garbin EVO ventilators (all software versions except 1.05.06.00) sold outside the US due to potential sudden loss of ventilation from battery or power alarms when 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 Garbin EVO ventilators sold outside the US (except software version 1.05.06.00) because they may lose ventilation suddenly due to battery or power alarms when the device actually has power. This could be dangerous for patients using the ventilator.
The ventilator may show a battery depleted or power loss alarm even when it has sufficient power. This can cause sudden loss of ventilation, which is dangerous for patients who rely on the device to breathe.
Patients using Garbin EVO ventilators for pediatric or adult care who own the recalled units (sold outside the US) are most at risk. The recall affects specific model numbers and serial numbers listed in the notice.
Check if your Garbin EVO ventilator has a model number starting with LD2110X23B or a serial number listed in the provided list (e.g., H252356907DD7, H2612106781C2, etc.). The device was sold outside the US and does not include software version 1.05.06.00.
Verify your Garbin EVO ventilator's model number starts with LD2110X23B and has a serial number from the list provided in the recall notice.
If you have the recalled device, contact Philips Respironics directly for instructions on how to address the issue.
Yes, if your ventilator has a model number starting with LD2110X23B and a serial number from the list provided in the recall notice, and was sold outside the US (excluding software version 1.05.06.00).
Contact Philips Respironics directly for instructions on how to address the issue. The recall does not include software version 1.05.06.00.
The recall states there is a potential for sudden loss of ventilation, which could be dangerous for patients using the ventilator. However, the remedy does not specify immediate action to stop use.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1500-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1500-2024 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.
