Philips Respironics recalls V60 Ventilators with part number R1053618 due to potential backup battery failure if over-discharged or stored without AC power. Affected units may require battery replacement.
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 R1053618 because their backup batteries can fail if the device is over-discharged or stored without being plugged in. This could lead to the ventilator not working properly during emergencies.
The ventilator's backup battery can fail if the device is left over-discharged or stored without being plugged into AC power for long periods. This could cause the ventilator to stop working during critical medical situations.
People using Philips Respironics V60 Ventilators with part number R1053618 for medical breathing support are affected. Those with respiratory conditions requiring ventilator assistance are at higher risk.
Check for part number R1053618 on the ventilator. The product was sold in Japan with model codes CFLEX and AVAPS. Serial numbers 100039155, 100054624, and 100054738 are affected.
Ensure the ventilator is plugged into AC power regularly to prevent over-discharge.
Reach out to Respironics California for specific guidance on battery replacement or repair.
No, only specific units with part number R1053618 and serial numbers 100039155, 100054624, and 100054738 are affected.
Check for part number R1053618 on the device. Affected units were sold in Japan with model codes CFLEX and AVAPS.
No, but you should ensure the device is plugged into AC power regularly to prevent battery failure.
We’ve drafted a message you can send Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0892-2021 — Respironics Respironics Hello, I own a Respironics that is covered by recall Z-0892-2021 from 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.
