Philips Respironics recalls A-Series BiPAP Hybrid A30 and V30 devices made before April 2021 due to potential PE-PUR foam particles entering airways. Affected units have specific serial numbers and material codes.
The polyester-based polyurethane (PE-PUR) foam may degrade into particles which may enter the devices air pathway and be ingested or inhaled by the user, and the PE-PUR foam may off-gas certain chemicals.
Philips Respironics is recalling certain A-Series BiPAP ventilators made before April 2021 because the foam used in their construction could break into particles that might be inhaled by users. This poses a risk of respiratory issues if the particles enter the air pathway.
The polyester-based polyurethane (PE-PUR) foam in these devices can degrade into small particles that may enter the air pathway and be inhaled or ingested by the user. Additionally, the foam may release certain chemicals that could pose health risks.
Users of the A-Series BiPAP Hybrid A30 and V30 ventilators made before April 2021 are most at risk. These devices are typically used by people with breathing difficulties who rely on ventilators for medical support.
Check if your device was manufactured before April 2021. Look for specific serial numbers and material codes listed in the recall notice: 1111181, 1111182, 1111178, 1140184, 1135427, 1143671.
Look for the serial number on your device to confirm if it matches the listed numbers: 1111181, 1111182, 1111178, 1140184, 1135427, 1143671.
No, these devices are not marketed in the US.
The recall does not specify a remedy, so contact Philips Respironics directly for guidance.
Check if your device was manufactured before April 2021 and has one of the listed serial numbers: 1111181, 1111182, 1111178, 1140184, 1135427, 1143671.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1957-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1957-2021 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.
