Reported Feb 3, 2021 · Ongoing

Philips Respironics V60 Ventilator Part Number 1053615 - 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 1053615 - 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 Number1053615 V60 Ventilator
  • Intl OptNone
  • Serial numbers

    934 of 934 codes

    • 100011125
    • 100021457
    • 100049066
    • 100049185
    • 100049195
    • 100049196
    • 100049200
    • 100122592
    • 100172279
    • 201003463
    • 100011045
    • 100013970
    • 100013971
    • 100015382
    • 100097294
    • 100106739
    • 100109494
    • 100109498
    • 100109499
    • 100109504
    • 100110679
    • 100120770
    • 100036303
    • 100036437
    • 100036446
    • 100036447
    • 100036452
    • 100120864
    • 100085138
    • 100101080
    • 100160827
    • 100006791
    • 100006794
    • 100006805
    • 100007128
    • 100007199
    • 100007208
    • 100007342
    • 100010908
    • 100011086
    • 100011088
    • 100011089
    • 100011090
    • 100011124
    • 100011127
    • 100011187
    • 100013251
    • 100013252
    • 100013253
    • 100013254
    • 100013255
    • 100013256
    • 100013282
    • 100013934
    • 100014019
    • 100014024
    • 100014518
    • 100015338
    • 100015342
    • 100015343
Amount recalled
934 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, 6:27 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.