Reported Feb 3, 2021 · Ongoing

Philips Respironics V60 Ventilator Part Number 1076709 - 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 1076709 - Product Usageintended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories
Lot codes and dates
  • ModelV60
  • Part Number1076709 V60 Ventilator
  • JAPAN OPTCFLEX,AVAPS,AT+
  • Serial Numbers

    2,955 of 2,955 codes

    • 100058561
    • 100058562
    • 100058565
    • 100058572
    • 100058573
    • 100058574
    • 100058576
    • 100058835
    • 100058840
    • 100058844
    • 100058845
    • 100058846
    • 100058902
    • 100058903
    • 100058904
    • 100058905
    • 100058906
    • 100058908
    • 100058911
    • 100058914
    • 100058917
    • 100058968
    • 100058970
    • 100058971
    • 100058975
    • 100058977
    • 100058990
    • 100058991
    • 100058994
    • 100058997
    • 100058999
    • 100059002
    • 100059149
    • 100059153
    • 100059163
    • 100059239
    • 100059248
    • 100060123
    • 100060124
    • 100060214
    • 100060215
    • 100060216
    • 100060219
    • 100060220
    • 100060222
    • 100060229
    • 100060232
    • 100060234
    • 100060236
    • 100060239
    • 100060328
    • 100060329
    • 100060330
    • 100060331
    • 100060339
    • 100060340
    • 100060341
    • 100060344
    • 100060345
    • 100060346
Amount recalled
3,752 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

  • Nationwide
  • PR

Why it was recalled

Potential issues with ventilator navigation ring interface and liquid ingress: 1) The navigation ring may become inoperative or operate intermittently; 2) The navigation ring may cause ventilator parameter values to change erratically during setting entries and adjustments.

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

Data as of Sep 19, 4:56 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.