Philips Respironics recalls BiPAP A30 Ventilators with specific part numbers (US and OUS) due to potential interruption of therapy, which may lead to hypoventilation, hypoxemia, hypercarbia, respiratory failure, or death in vulnerable patients.
Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.
Philips Respironics is recalling BiPAP A30 Ventilators with specific part numbers (US and OUS) because they can experience interruptions in therapy, which may cause hypoventilation, hypoxemia, hypercarbia, respiratory failure, or death in patients with breathing difficulties. This is a serious risk for individuals who rely on these devices.
The ventilator may experience interruptions in therapy during the 'Ventilator Inoperative' alarm, which can lead to hypoventilation (inadequate breathing), hypoxemia (low oxygen levels), hypercarbia (high carbon dioxide levels), respiratory failure, or potentially death in patients who rely on the device for breathing support.
Patients using the BiPAP A30 Ventilator for breathing support are most at risk, particularly those with respiratory conditions who depend on continuous therapy. The recall affects specific part numbers sold in the US and other countries.
Check if your device has part numbers listed in the recall (e.g., 1111143 for US, or specific OUS numbers like 1111144-1111149). The recall includes both US and international distribution with specific serial numbers and material numbers.
Verify your BiPAP A30 Ventilator's part number against the list of affected numbers provided in the recall.
Reach out to Philips Respironics for guidance on next steps, as the recall does not include a specific remedy or replacement.
The recall affects specific part numbers including 1111143 (US), and OUS numbers 1111144-1111149, 1111150, 1111154, 1111181, 1116155, 1111144L, 1111144M, 1111144V, BR1111143, CN1111143, R1111143, R1111150, R1111181, and many others as listed in the recall.
No, the recall does not require immediate discontinuation. However, patients should monitor for therapy interruptions and contact Philips Respironics for guidance.
The recall does not specify a remedy or replacement. Affected users should contact Philips Respironics directly for assistance.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1814-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1814-2024 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.
