Philips Respironics recalls V60 Ventilators with part number R1053618 due to navigation ring issues causing erratic settings. Affected units may need repair or replacement.
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 R1053618 because the navigation ring can become inoperative or cause settings to change erratically. This could lead to incorrect ventilator adjustments, which might affect patient safety.
The navigation ring on the ventilator can malfunction or cause settings to change unexpectedly during adjustments. This could lead to incorrect ventilator settings, potentially affecting patient breathing safety.
People using Philips Respironics V60 Ventilators with part number R1053618 for medical breathing support are affected. Patients and caregivers who rely on this ventilator for respiratory assistance are most at risk.
Check for part number R1053618 on the ventilator. Affected units were sold with serial numbers 100039155, 100054624, and 100054738.
Ensure the navigation ring is functioning correctly and settings are stable before use.
Reach out to Respironics California for repair or replacement options.
The navigation ring may become inoperative or cause ventilator settings to change erratically, which could affect patient safety.
Part number R1053618 for Philips Respironics V60 Ventilators.
Check for part number R1053618 and serial numbers 100039155, 100054624, or 100054738.
We’ve drafted a message you can send Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0909-2021 — Respironics Respironics Hello, I own a Respironics that is covered by recall Z-0909-2021 from 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.
