Philips Respironics recalls BiPAP A40 Ventilators that are not indicated for use in patients with respiratory failure. Affected units have specific serial numbers. Consumers should stop using if they have the device and contact Philips for details.
This device does not indicate for use in patients with respiratory failure.
Philips Respironics is recalling BiPAP A40 Ventilators that are not intended for use in patients with respiratory failure. This means the device could be unsafe for people who need respiratory support, as it may not function properly in critical cases. If you own this device, stop using it immediately and contact Philips for instructions.
The BiPAP A40 Ventilator is not indicated for use in patients with respiratory failure. This means it may not function correctly or safely for individuals who require respiratory support in critical conditions, potentially leading to inadequate treatment.
Patients using the BiPAP A40 Ventilator for respiratory support, particularly those with respiratory failure, are at risk. The device is not designed for this purpose, so it may not provide adequate treatment.
Check if your device has the serial numbers listed in the recall: V182393118CC9, V21942863DD70, V219429359C22, and others (the full list is provided in the recall).
If you have the recalled BiPAP A40 Ventilator, stop using it immediately.
Philips Respironics is recalling BiPAP A40 Ventilators that are not indicated for use in patients with respiratory failure.
Check if your device has the serial numbers listed in the recall, such as V182393118CC9, V21942863DD70, V219429359C22, and others from the provided list.
Stop using the device immediately and contact Philips Respironics for further instructions.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-2037-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-2037-2025 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.
