Philips Respironics recalls V60 Ventilators with part number 1076717 due to navigation ring issues that may cause erratic ventilator settings. Affected units have specific serial numbers.
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 1076717 because the navigation ring may become inoperative or cause settings to change erratically. This could lead to incorrect ventilator adjustments during use, potentially affecting patient safety.
The navigation ring on the ventilator may stop working or change settings unpredictably. This could cause the ventilator to adjust patient breathing parameters incorrectly during use, which might lead to unsafe conditions.
Patients using the Philips Respironics V60 Ventilator with part number 1076717 are most at risk. The recall affects specific units with listed serial numbers.
Check if your ventilator has part number 1076717 and serial numbers listed in the provided range (e.g., 100033299 to 100036149). The product is intended for use with Respironics-recommended patient circuits and accessories.
Verify if the navigation ring is functioning correctly and settings are stable before use.
Reach out to Philips Respironics for guidance on potential fixes or alternatives if issues persist.
The recalled ventilator has part number 1076717.
Affected serial numbers range from 100033299 to 100036149 as listed in the recall notice.
The recall does not specify a fix; users should contact Philips Respironics for guidance.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0912-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0912-2021 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.
