Reported Feb 3, 2021 · Ongoing

Philips Respironics V680 Ventilator Part Number 850011 - 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 V680 Ventilator
  • Part Number 850011 - Product Usageintended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories
Lot codes and dates
  • ModelV680
  • Part Number850011 V680 Ventilator
  • Finished Serial Numbers

    2,947 of 2,947 codes

    • 201009427
    • 201009428
    • 201009429
    • 201009493
    • 201009494
    • 201009495
    • 201009496
    • 201009498
    • 201009499
    • 201009660
    • 201009661
    • 201009662
    • 201009663
    • 201009664
    • 201009665
    • 201009666
    • 201009667
    • 201009668
    • 201009669
    • 201009670
    • 201009671
    • 201009672
    • 201009673
    • 201009675
    • 201009676
    • 201009677
    • 201009678
    • 201009679
    • 201009674
    • 201008743
    • 201008765
    • 201008766
    • 201008770
    • 201008771
    • 201008776
    • 201008785
    • 201008786
    • 201008805
    • 201009497
    • 201008801
    • 201008741
    • 201008744
    • 201008760
    • 201008764
    • 201008767
    • 201008768
    • 201008772
    • 201008775
    • 201008783
    • 201008808
    • 201008762
    • 201008773
    • 201008781
    • 201008809
    • 201008807
    • 100124645
    • 100124646
    • 100125009
    • 100125011
    • 100125012
Amount recalled
3,453 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.