Reported Jul 29, 2020 · Ongoing

IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391,…

Philips North America, 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: Philips North America, LLC · 3000 Minuteman Rd · Andover, MA · 01810-1032

Is this the product you have?

    • IntelliVue G7m Anesthesia Gas Module
    • Model no. 866173
    • Firmware Version 04.12.00
    • System Codes 453564477391
    • 453564477401
    • 866173
Lot codes and dates
  • Serial numbers

    2,716 of 2,716 codes

    • DE43804813
    • DE43804952
    • DE43804945
    • DE43806034
    • DE43806054
    • DE43803806
    • DE43803822
    • DE43803824
    • DE43803907
    • DE43803911
    • DE43803915
    • DE43803983
    • DE43803986
    • DE43803988
    • DE43803989
    • DE43806224
    • DE43803973
    • DE43803895
    • DE43804009
    • DE43803778
    • DE43803752
    • DE43803762
    • DE43803766
    • DE43803772
    • DE43803773
    • DE43803774
    • DE43803790
    • DE43805609
    • DE43804358
    • DE43804391
    • DE43805722
    • DE43804085
    • DE43804093
    • DE43803753
    • DE43803754
    • DE43803769
    • DE43803823
    • DE43803831
    • DE43803836
    • DE43803841
    • DE43805272
    • DE43805280
    • DE43805291
    • DE43805295
    • DE43803802
    • DE43803812
    • DE43803814
    • DE43803815
    • DE43803826
    • DE43803828
    • DE43805705
    • DE43805709
    • DE43805713
    • DE43805717
    • DE43805720
    • DE43805725
    • DE43805735
    • DE43805744
    • DE43805515
    • DE43805516
Amount recalled
3075

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

The device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and display of gas levels and generating one or more technical or INOP alarms.

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.

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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, 6:50 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.