Reported Feb 3, 2021 · Terminated

Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage: intended to be used only with various…

Respironics California, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Respironics California, LLC · 2271 Cosmos Ct · Carlsbad, CA · 92011-1517

Is this the product you have?

  • Philips Respironics V60 Ventilator
  • Part Number 1053618 - Product Usageintended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories
Lot codes and dates
  • Model
    • V60 Ventilator
    • Part Number 1053618 V60 Ventilator
  • Japan OptCFLEX
  • AVAPS Serial Numbers

    534 of 534 codes

    • 100019618
    • 100019631
    • 100019639
    • 100019822
    • 100019823
    • 100019824
    • 100019827
    • 100019838
    • 100019917
    • 100019920
    • 100019922
    • 100019924
    • 100019965
    • 100019966
    • 100019967
    • 100019971
    • 100019972
    • 100020663
    • 100020664
    • 100020665
    • 100020666
    • 100022148
    • 100023892
    • 100023893
    • 100023894
    • 100023896
    • 100023897
    • 100023899
    • 100023905
    • 100023909
    • 100023940
    • 100023941
    • 100023944
    • 100023956
    • 100023995
    • 100023998
    • 100024000
    • 100024003
    • 100024007
    • 100024008
    • 100024688
    • 100025546
    • 100025549
    • 100026087
    • 100026088
    • 100026089
    • 100026090
    • 100026092
    • 100026095
    • 100026124
    • 100027090
    • 100027095
    • 100027100
    • 100027101
    • 100027108
    • 100027114
    • 100027174
    • 100027176
    • 100027181
    • 100027185
Amount recalled
534 systems

This recall covers 33 products

The agency filed one notice per product. You are reading one of them; the other 32 are below.

20 more are in the archive.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 19, 2024 · Data as of Sep 19, 5:39 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.