Reported Feb 3, 2021 · Ongoing

Philips Respironics V60 Ventilator Part Number R1076709 - 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 R1076709 - 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 NumberR1076709 V60 Ventilator
  • JAPAN OPTCFLEX,AVAPS,AT+
  • Serial Numbers

    2,955 of 2,955 codes

    • 100065352
    • 100065365
    • 100065371
    • 100065487
    • 100065493
    • 100067423
    • 100067425
    • 100067428
    • 100067431
    • 100067451
    • 100068214
    • 100069518
    • 100070301
    • 100070306
    • 100070398
    • 100070476
    • 100070491
    • 100070492
    • 100070768
    • 100070774
    • 100070776
    • 100070777
    • 100070778
    • 100070780
    • 100070781
    • 100070859
    • 100070862
    • 100070865
    • 100070921
    • 100070922
    • 100070924
    • 100070928
    • 100070929
    • 100070930
    • 100070935
    • 100070966
    • 100070969
    • 100070973
    • 100070976
    • 100070981
    • 100071071
    • 100071073
    • 100071077
    • 100071123
    • 100071461
    • 100071510
    • 100071511
    • 100072415
    • 100072417
    • 100072418
    • 100072499
    • 100072570
    • 100072606
    • 100072607
    • 100072673
    • 100072676
    • 100072679
    • 100072684
    • 100072685
    • 100072688
Amount recalled
3213 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, 7:01 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.