RecallRadar

FDA Device recall Z-2531-2020

Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MM…

On 2020-07-15 the FDA classified a Class II recall of Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MM… by Philips North America, citing affected M3015A extensions are incompatible with the lntelliVue X3 Patient Monitor (Model No. 867030) and lntelliVue MMX multi-measurement server (Model No. 867036).If they are co….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2531-2020
ClassificationClass II
Statusterminated
Initiated2020-06-08
Published2020-07-15
Last updated2026-09-13 11:55 UTC
CompanyPhilips North America
DistributionUS

Product

Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MMX Multi-Measurement Module (Model No. 867036)

Reason

Affected M3015A extensions are incompatible with the lntelliVue X3 Patient Monitor (Model No. 867030) and lntelliVue MMX multi-measurement server (Model No. 867036).If they are connected to a host monitor, communication with the X3 or MMX could be disrupted, resulting in a loss of monitoring on the host monitor.

Identifiers

code_infoUnits with this hardware version can be identified by the following serial number prefix: SN prefix: DE435xxxxx (first five digits)

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2531-2020%22

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