Reported Feb 3, 2021 · Ongoing

Philips Respironics V60 Ventilator Part Number 1076716 - 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 1076716 - 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 Number1076716 V60 Ventilator
  • CHINA OPTCFLEX
  • AVAPS Serial Numbers

    2,955 of 2,955 codes

    • 100193935
    • 100194169
    • 100030124
    • 100030335
    • 100030359
    • 100030360
    • 100030761
    • 100030762
    • 100030763
    • 100030764
    • 100030766
    • 100030767
    • 100030768
    • 100030769
    • 100030770
    • 100030771
    • 100030773
    • 100030775
    • 100030776
    • 100030777
    • 100030779
    • 100030782
    • 100030783
    • 100030784
    • 100032461
    • 100032686
    • 100032687
    • 100032688
    • 100032689
    • 100032690
    • 100032691
    • 100032692
    • 100032695
    • 100032697
    • 100032698
    • 100032701
    • 100032702
    • 100035773
    • 100035778
    • 100035779
    • 100035896
    • 100035897
    • 100035898
    • 100035899
    • 100035900
    • 100035901
    • 100035902
    • 100035903
    • 100035904
    • 100035907
    • 100035909
    • 100035910
    • 100035911
    • 100035913
    • 100035914
    • 100035918
    • 100035919
    • 100035926
    • 100036047
    • 100036302
    1
Amount recalled
10,291 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, 7:04 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.