Reported Feb 3, 2021 · Ongoing

Philips Respironics V60 Ventilator Part Number 1137292 - 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 1137292 - 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 Number
    • 1137292 V60 Ventilator
    • Intl Opt CFLEX
    • AVAPS 3.00
  • SW Serial Numbers

    834 of 834 codes

    • 100286055
    • 100286057
    • 100286203
    • 100286204
    • 100286207
    • 100289426
    • 100289690
    • 100289701
    • 100289702
    • 100289703
    • 100289704
    • 100289711
    • 100291365
    • 100291472
    • 100291487
    • 100291842
    • 100309654
    • 100309725
    • 100309726
    • 100309728
    • 100311169
    • 100311171
    • 100314702
    • 100315038
    • 100318590
    • 100318593
    • 100318613
    • 100319271
    • 100319286
    • 100319296
    • 100319298
    • 100319300
    • 100329969
    • 100329972
    • 100329979
    • 100337251
    • 100339218
    • 100340917
    • 100341273
    • 100345558
    • 100345603
    • 100369688
    • 100284364
    • 100284366
    • 100286200
    • 100286201
    • 100286202
    • 100286206
    • 100288337
    • 100289430
    • 100289495
    • 100289498
    • 100289684
    • 100289700
    • 100291197
    • 100291363
    • 100291364
    • 100291370
    • 100291468
    • 100291473
Amount recalled
834 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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Respironics California, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:59 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.