Philips Respironics recalls V60 Ventilators (Part 1137292) due to navigation ring interface problems that may cause erratic parameter changes during adjustments. Affected units have specific serial numbers listed in the recall.
Potential issues with ventilator navigation ring interface and liquid ingress: 1) The navigation ring may become inoperative or operate intermittently; 2) The navigation ring may cause ventilator parameter values to change erratically during setting entries and adjustments.
Philips Respironics is recalling V60 Ventilators with part number 1137292 because the navigation ring interface can become inoperative or cause parameter values to change erratically during adjustments. This could lead to improper ventilator settings for patients.
The navigation ring interface may become inoperative or operate intermittently, causing ventilator parameter values to change unexpectedly during setting entries and adjustments. This could lead to improper ventilator settings for patients.
Patients using the Philips Respironics V60 Ventilator with part number 1137292 are most at risk. The recall affects specific units with listed serial numbers.
Check if your V60 Ventilator has part number 1137292 and serial numbers listed in the provided list (e.g., 100286055, 100286057, etc.).
Verify your V60 Ventilator has part number 1137292 and a serial number from the list provided in the recall.
If you have the recalled unit, contact Philips Respironics for further instructions on how to address the issue.
The part number is 1137292.
Check if your V60 Ventilator has part number 1137292 and a serial number from the list provided in the recall.
Contact Philips Respironics for further instructions on how to address the issue.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0914-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0914-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
