Philips Respironics recalls V60 Ventilators with part number U1053617 due to potential backup battery failure from over-discharge or extended storage without 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 part number U1053617 because the backup battery may fail if the device is over-discharged or stored without power for long periods. This could lead to the ventilator not working properly when needed.
The backup battery may fail if the ventilator is over-discharged or stored without being plugged into AC power for an extended period. This could cause the device to stop working when needed during critical medical situations.
People using Philips Respironics V60 Ventilators with part number U1053617 are affected. Those with respiratory conditions requiring ventilator support are most at risk.
Check for the part number U1053617 on your V60 Ventilator. The serial numbers listed in the recall include a range of numbers starting with 100000000 and ending with 201031987.
Ensure your ventilator is plugged into AC power regularly to prevent battery over-discharge.
The recall addresses potential backup battery failure, but the risk is low. The ventilator may not work properly if the battery fails, but serious injury is not expected.
Check for the part number U1053617 on your V60 Ventilator. The serial numbers listed in the recall include a range of numbers starting with 100000000 and ending with 201031987.
The recall does not specify a remedy, but you should ensure your ventilator is plugged into AC power regularly to prevent battery over-discharge.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0900-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0900-2021 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.
