Philips Respironics V60 Ventilators with Japanese language and NIST oxygen fittings may have contaminated gas pathways. Recalled units include specific model numbers and serials. Contact for remedy.
Devices were imported with Japanese Language and NIST Oxygen Gas Fittings and retrofitted, may pose a serious health risk as the gas pathway of these devices may be contaminated.
Philips Respironics V60 Ventilators were recalled because they were retrofitted with Japanese language and NIST oxygen fittings that could contaminate the gas pathway, posing a serious health risk. This affects patients using the device for breathing assistance.
The ventilators were retrofitted with Japanese language and NIST oxygen fittings that may contaminate the gas pathway. This contamination could lead to serious health risks for patients relying on the device for breathing assistance.
Patients using Philips Respironics V60 Ventilators for breathing assistance are most at risk. The recall applies to specific model numbers and serials sold in the U.S.
Check for model numbers R1053618 or R1076709 and serial numbers listed in the recall notice. These units were imported with Japanese language and NIST oxygen fittings and retrofitted.
Immediately stop using the recalled Philips Respironics V60 Ventilator if you have the specific model numbers or serials listed in the recall.
The ventilators were retrofitted with Japanese language and NIST oxygen fittings that may contaminate the gas pathway, posing a serious health risk.
Model numbers R1053618 and R1076709 with specific serial numbers listed in the recall notice.
Stop using it now 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-2025-2023 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-2025-2023 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.
