Philips recalls M3015A Microstream CO2 Extension Model 862393 used with X3 Patient Monitor (Model 867030) or MMX server (Model 867036) due to communication disruption risk.
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.
Philips is recalling M3015A Microstream CO2 Extension Model 862393 that may not work with certain patient monitors. This could cause loss of monitoring if connected to an X3 or MMX server, potentially affecting patient safety.
The M3015A extension may not communicate properly with the X3 Patient Monitor or MMX server. This could cause temporary loss of monitoring data on the host device, potentially delaying critical patient care.
Healthcare professionals using Philips M3015A extensions with X3 Patient Monitors (Model 867030) or MMX servers (Model 867036) are most at risk. Patients connected to these systems could experience monitoring disruptions.
Check for the serial number prefix DE435xxxxx on the extension. The product is sold with X3 Patient Monitors (Model 867030) or MMX servers (Model 867036).
Verify if your M3015A extension works with your X3 Patient Monitor (Model 867030) or MMX server (Model 867036) by checking the serial number prefix.
The M3015A extension may not communicate properly with certain patient monitors, causing temporary loss of monitoring data.
Look for the serial number prefix DE435xxxxx on the extension. It was sold with X3 Patient Monitors (Model 867030) or MMX servers (Model 867036).
No, but you should check compatibility with your monitor to avoid potential monitoring disruptions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2531-2020 — Philips Philips Hello, I own a Philips that is covered by recall Z-2531-2020 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
