Philips Respironics V60 Ventilator (Part 1053616) recalled due to potential backup battery failure if over-discharged or stored without AC 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 1053616 because the backup battery can 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 backup battery may fail if the ventilator is left without power for too long or if the battery is over-discharged. This could cause the device to stop working during critical medical use.
People using the Philips Respironics V60 Ventilator with part number 1053616 are affected. Those who rely on this device for medical breathing support are most at risk if the ventilator fails.
Check if your ventilator has the part number 1053616 and serial numbers listed in the recall notice (e.g., 100087733, 100087738, etc.).
Ensure your ventilator is plugged into AC power regularly to prevent battery over-discharge.
The ventilator is safe if used with regular AC power connections and not stored without power for extended periods.
Check if your ventilator has part number 1053616 and one of the listed serial numbers (e.g., 100087733, 100087738, etc.).
The recall does not require returning the ventilator; users should ensure regular power connections to prevent battery failure.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0888-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0888-2021 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.
