Philips Respironics recalls V60 Ventilators with specific model numbers and serials due to potential internal electrical circuit issues that could cause the device to stop operating. Affected users should check their model and serial numbers.
Ventilator units have an issue impacting an internal electrical circuit within the ventilators, that in some cases could result in the ventilator ceasing to operate.
Philips Respironics is recalling all V60 Ventilators with specific model numbers and serials because an internal electrical circuit issue might cause the ventilator to stop working. This could affect users who rely on the device for breathing support.
The ventilator has an internal electrical circuit issue that could cause it to stop working. This might happen in some cases, but it does not typically cause serious injury or death.
People using Philips Respironics V60 Ventilators with the listed model numbers and serials are affected. Those who rely on the ventilator for breathing support are most at risk.
Check the model numbers and serial numbers listed in the recall notice. The affected units include specific model numbers like 1053613 through 1053618 and serial numbers starting with 00884838009844.
Look for the model numbers and serial numbers listed in the recall notice to confirm if your ventilator is affected.
The recall does not require immediate stop use; the issue is unlikely to cause serious injury but may cause the device to stop working.
Affected model numbers include 1053613 through 1053618 and serial numbers starting with 00884838009844.
The recall does not specify a remedy, so affected users should contact Philips Respironics for further instructions.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0907-2022 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0907-2022 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.
