Reported Feb 3, 2021 · Ongoing

Philips Respironics V60 Plus Ventilator Part Number 1137276 - 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 Plus Ventilator
  • Part Number 1137276 - 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
  • Plus Part Number1137276 V60 Plus Ventilator
  • International Serial Numbers

    2,955 of 2,955 codes

    • 100341890
    • 100341897
    • 100343602
    • 100343674
    • 100345138
    • 100345145
    • 100345148
    • 100352752
    • 100352754
    • 100354448
    • 100354454
    • 100354464
    • 100354470
    • 100354838
    • 100354875
    • 100357792
    • 100358141
    • 100358158
    • 100358355
    • 100359515
    • 100381237
    • 100381430
    • 100381436
    • 100381765
    • 100381835
    • 100381850
    • 100384222
    • 100384818
    • 100384821
    • 100384875
    • 100384878
    • 100384903
    • 100387138
    • 100387261
    • 100387407
    • 100387412
    • 100387557
    • 100387860
    • 100387941
    • 100387953
    • 100388063
    • 100388068
    • 100388092
    • 100388630
    • 100388634
    • 100388640
    • 100388641
    • 100388649
    • 100388676
    • 201040204
    • 201040216
    • 100345306
    • 100345307
    • 100346866
    • 100346876
    • 100346889
    • 100346894
    • 100346895
    • 100346896
    • 100346898
    1
Amount recalled
3,841 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, 4:57 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.