Philips Respironics recalls V60 Ventilators with part number 1053613 due to potential navigation ring interface problems that may cause intermittent operation and parameter changes.
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 1053613 because the navigation ring interface may become inoperative or cause erratic changes in ventilator settings. This could lead to incorrect patient settings during adjustments.
The navigation ring interface may become inoperative or operate intermittently, causing the ventilator to change settings unexpectedly during adjustments. This could lead to incorrect patient ventilation parameters.
Patients using this ventilator for medical treatment are most at risk, particularly those who rely on precise settings for respiratory support.
Check for part number 1053613 on the ventilator. The model is V60 with international options CFLEX, AVAPS, and PP. Serial numbers listed in the recall include a range of numbers starting with 100029460 through 100392695.
Verify if the navigation ring is functioning correctly and if settings are stable during adjustments.
Reach out to Philips Respironics for guidance on potential fixes or replacements.
No, only specific models with part number 1053613 and the listed serial numbers are affected.
Check the part number on your ventilator; if it's 1053613 and your serial number is in the list provided, it's affected.
Contact Philips Respironics for guidance on potential fixes or replacements, as the recall does not specify a replacement process.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0902-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0902-2021 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.
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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.
