Philips Respironics recalls V60 Ventilators with part number 1076717 due to potential backup battery failure if over-discharged or stored without power. Affected units have specific serial numbers.
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 part number 1076717 because the backup battery may fail if the device is over-discharged or stored without being plugged in. This could lead to the ventilator not working properly when needed.
The ventilator's backup battery may fail if it's over-discharged or if the device is stored without being plugged into AC power for a long time. This could cause the ventilator to stop working when needed.
People using Philips Respironics V60 Ventilators with part number 1076717 are affected. Those with specific serial numbers listed in the recall are most at risk.
Check if your ventilator has part number 1076717 and the listed serial numbers (e.g., 100033299 to 100036149). The product is intended for use with Respironics-recommended accessories.
Look for the serial number on your ventilator's label to see if it matches the list of affected numbers provided in the recall.
The backup battery may fail if the ventilator is over-discharged or stored without being plugged into AC power for an extended period.
Check if your ventilator has part number 1076717 and a serial number from the list provided in the recall (e.g., 100033299 to 100036149).
No action is needed if your ventilator's serial number is not listed 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-0895-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0895-2021 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.
