Philips Respironics recalls V60 Ventilators with part number 1053616 due to potential navigation ring interface problems that may cause erratic ventilator parameter changes during adjustments.
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 1053616 because the navigation ring interface may become inoperative or cause parameter values to change erratically during adjustments. This could lead to incorrect ventilator settings for patients using the device.
The navigation ring interface may become inoperative or operate intermittently, causing ventilator parameter values to change erratically during setting entries and adjustments. This could lead to incorrect ventilator settings for patients.
Patients using the Philips Respironics V60 Ventilator with part number 1053616 are most at risk. The device is intended for medical use with specific patient circuits and interfaces.
Check for the model V60 with part number 1053616. Serial numbers listed in the recall include many numbers starting with 1000 and 20100.
Verify if your ventilator has the part number 1053616 and the listed serial numbers.
Reach out to Philips Respironics for replacement or repair options.
Check if your ventilator has part number 1053616 and the listed serial numbers to see if it's affected.
Contact Philips Respironics for replacement or repair options.
Look for the model V60 with part number 1053616 and check the serial numbers against the list provided in the recall.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0905-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0905-2021 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.
