Reported Feb 3, 2021 · Ongoing

Philips Respironics V60 Ventilator Part Number 1076717 - 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 1076717 - 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 Number1076717 V60 Ventilator
  • CHINA OPTNONE
  • Serial Numbers

    216 of 216 codes

    • 100033299
    • 100033300
    • 100033301
    • 100033302
    • 100033303
    • 100033304
    • 100033305
    • 100033306
    • 100033308
    • 100033309
    • 100033310
    • 100033311
    • 100033312
    • 100033313
    • 100033314
    • 100033315
    • 100033316
    • 100033317
    • 100033318
    • 100033319
    • 100033320
    • 100033321
    • 100033322
    • 100033323
    • 100033562
    • 100033563
    • 100033564
    • 100033565
    • 100033566
    • 100033567
    • 100033568
    • 100033569
    • 100033570
    • 100033571
    • 100033572
    • 100033573
    • 100033574
    • 100033575
    • 100033576
    • 100033577
    • 100033578
    • 100033579
    • 100033580
    • 100033581
    • 100033582
    • 100033583
    • 100033584
    • 100033585
    • 100033586
    • 100033587
    • 100033588
    • 100033589
    • 100033590
    • 100033591
    • 100033592
    • 100033593
    • 100033594
    • 100033595
    • 100033645
    • 100033646
Amount recalled
216 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, 7:48 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.