Philips Respironics recalls V60 Ventilators with serial numbers starting 100002908 to 100040856. These units may experience backup battery failures if over-discharged or stored without AC power.
Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
Philips Respironics is recalling V60 Ventilators with specific serial numbers due to potential backup battery failures. If the battery is over-discharged or the ventilator is stored without AC power for extended periods, it could malfunction.
The ventilator's backup battery may fail if the device is left uncharged for long periods or if the battery is drained completely. This could cause the ventilator to stop working during a power outage, potentially affecting breathing support.
People using Philips Respironics V60 Ventilators with the listed serial numbers are affected. Those with respiratory conditions requiring ventilator support are at higher risk.
Check if your ventilator has a serial number starting with 100002908 through 100040856. The product is a Philips Respironics V60 Ventilator with part number DU1053617.
Ensure your ventilator is connected to AC power and the battery is not over-discharged.
If you experience unexpected shutdowns or breathing difficulties, contact Philips Respironics immediately.
Check if your ventilator has a serial number starting with 100002908 through 100040856. If so, it is affected.
Keep the ventilator plugged into AC power regularly and avoid letting the battery over-discharge.
The recall does not require battery replacement; proper usage and monitoring are sufficient.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0899-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0899-2021 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.
