Philips Respironics recalls several ventilator models due to potential release of harmful chemicals from polyester-based polyurethane foam.
The polyester-based polyurethane (PE-PUR) foam may degrade into particles which may enter the device s the air pathway and be ingested or inhaled by the user, and the PE-PUR foam may off-gas certain chemicals.
Philips Respironics is recalling multiple ventilator models because the foam used in their devices may degrade into particles that can be inhaled or ingested by users, and may off-gas harmful chemicals.
The polyester-based polyurethane foam in the ventilators can break down into particles that may be inhaled or swallowed by users, and can release harmful chemicals into the air.
Adults and children over 7 years old and 18kg weight who use these ventilators for respiratory support are affected. Those with respiratory insufficiency are most at risk.
Check if your ventilator has any of the listed serial numbers or material numbers in the recall notice. The devices are intended for adults and children over 7 years old and 18kg weight.
Look for the serial number on your ventilator's label or documentation to see if it matches the list of affected models provided in the recall.
The polyester-based polyurethane foam in these ventilators may degrade into particles that can be inhaled or ingested by users, and may off-gas harmful chemicals.
DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, C-Series ASV, C-Series S/T and AVAPS, OmniLab Advanced+ ventilators with the listed serial numbers or material numbers.
The recall does not require immediate stoppage; however, you should check if your device is affected and follow the provided steps to ensure safety.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1973-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1973-2021 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.
