Philips Respironics recalls V60/V60 Plus ventilators with specific PCBA part numbers due to potential power failure causing loss of function. Affected units may need replacement.
Power Management PCBAs may malfunction, causing a power failure leading to ventilator loss of function.
Philips Respironics is recalling V60 and V60 Plus ventilators with certain part numbers because faulty power management boards could cause the device to stop working. This poses a risk of the ventilator failing during use, which could be dangerous for patients relying on it.
The power management PCBAs in these ventilators may malfunction, causing the device to lose power and stop functioning. This could lead to the ventilator failing during critical use, potentially endangering patients who depend on it for breathing support.
Patients using Philips Respironics V60/V60 Plus ventilators with the specified part numbers are most at risk. The recall affects medical devices used by individuals with breathing conditions who require ventilator support.
Check for PCBA part number 453561544461 or V60 device part numbers 1053617 (US) and 1137276 (Philippines). Also look for specific serial numbers listed in the recall notice.
Identify your ventilator's PCBA part number and device part numbers to confirm if it is affected.
Reach out to Philips Respironics for guidance on next steps if your device is affected.
The power management PCBAs may malfunction, causing the ventilator to lose power and stop functioning, which could be dangerous for patients using it.
PCBA part number 453561544461 and V60 device part numbers 1053617 (US) and 1137276 (Philippines).
No, but you should check if your device is affected and 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-2631-2023 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-2631-2023 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.
