Philips Respironics recalls BiPAP A40 ventilators with non-conforming plastic that may release harmful VOCs and cause sudden failure. Affected units have specific serial numbers from China.
Certain devices were built with motor assemblies that could contain non-conforming plastic material. This could result in 1. Exposure to off-gassing of Volatile Organic Compounds not normally present creating a potential biosafety or toxicological hazard and 2. Sudden failure of the device causing a Ventilator Inoperative condition with the potential for asphyxia if not immediately identified and addressed by the care provider.
Philips Respironics is recalling certain BiPAP A40 ventilators due to plastic components that could release harmful chemicals and cause the device to stop working unexpectedly. This poses a risk of asphyxiation if not addressed by a healthcare provider.
The ventilators contain non-conforming plastic that may release volatile organic compounds (VOCs), creating a potential health hazard. If the device suddenly stops working, it could lead to asphyxiation if not immediately addressed by a healthcare provider.
Healthcare providers using the BiPAP A40 ventilators in medical settings are most at risk. Patients relying on these devices for breathing support could face sudden failure.
Check for serial numbers listed: V30446637ACAE, V30446653BE5A, V304441360854, V304457587F98, V304468408502, V304441766F34, V3044555732D7, V30446846E034, V30444034719A, V3044642346EA. These units were sold in China with the material number CN1111169.
Verify if your device has one of the listed serial numbers: V30446637ACAE, V30446653BE5A, V304441360854, V304457587F98, V304468408502, V304441766F34, V3044555732D7, V30446846E034, V30444034719A, V3044642346EA.
The ventilators contain non-conforming plastic that could release harmful chemicals and cause sudden failure.
Check if your device has one of the listed serial numbers. If it does, contact Philips Respironics for instructions.
Yes, if the device suddenly stops working, it could lead to asphyxiation if not immediately addressed by a healthcare provider.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1626-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1626-2021 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.
