Philips Respironics recalls specific OmniLab Advanced ventilator models (product numbers 1111122-1111142) due to potential interruption of therapy, which may lead to hypoventilation, hypoxemia, hypercarbia, respiratory failure, or death.
Device may experience an interruption or loss of therapy in case of a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death.
Philips Respironics is recalling specific OmniLab Advanced ventilator models (product numbers 1111122 through 1111142) because they may experience therapy interruptions, which could lead to hypoventilation, hypoxemia, hypercarbia, respiratory failure, or death. Affected users should stop using the device immediately.
The ventilator may experience an interruption or loss of therapy in response to the Ventilator Inoperative alarm. This can lead to hypoventilation (inadequate breathing), hypoxemia (low oxygen levels), hypercarbia (high carbon dioxide levels), respiratory failure, or potentially death if the device stops providing necessary breathing support.
Individuals with respiratory conditions who use the recalled OmniLab Advanced ventilators for breathing support are most at risk. The recall affects specific product numbers listed in the official notice.
Check if your ventilator has a product number listed in the official recall notice (1111122 through 1111142). The product numbers are also associated with specific serial numbers and UDI-DI codes provided in the recall list.
Immediately stop using the affected ventilator as it may cause life-threatening breathing issues.
The recall affects specific OmniLab Advanced ventilators with product numbers 1111122 through 1111142, as listed in the official notice.
Check your ventilator's product number against the list of affected product numbers (1111122 through 1111142) provided in the recall notice.
Immediately stop using the affected ventilator 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-1817-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1817-2024 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.
