Flexible Module Server FMX-4Recalls & reported problems

Philips Medizin Systeme Böblingen GmbH · The IntelliVue FMX-4 Flexible Module Rack provides 4 module slots for use with individual measurement modules and the recorder. The optional E20 Multi Measurement Module mount provides a mounting plate with an SRL connector for attaching a multi-measurement module. The FMX-4 is only compatible with IntelliVue MX750 and MX850 patient monitors. · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports: 3
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00884838086982), received between Dec 29, 2024 and May 28, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Defective Alarm” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Defective Alarm1
Fire1
Incorrect Measurement1

Patient problems

No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

MalfunctionMay 28, 2026Fire
PHILIPS RECEIVED A COMPLAINT ON A FLEXIBLE MODULE SERVER FMX-4 INDICATING THAT WHILE CONNECTED TO THE MACHINE, AN IV-BAG GOT RUPTURED AND THE CONTENTS GOT INTO THE CONNECTOR WHERE THE MXL CABLE CONNECTS AND CAUGHT ON FIRE. THE DEVICE WAS NOT IN USE ON PATIENT AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25315696 ↗
MalfunctionApr 9, 2026Incorrect Measurement
PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE FMX-4 INDICATING THAT THE ECG WAVE IS BEING CLIPPED. THE DEVICE WAS IN USE ON A PATIENT AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24831212 ↗
MalfunctionDec 29, 2024Defective Alarm; Defective Alarm
IT WAS REPORTED THE MONITOR DOES NOT GIVE A 3-STAR ALARM. IT COULD NOT BE READ FROM THE MONITOR. THE DEVICE WAS IN USE ON PATIENT AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21032266 ↗

Device details

UDI-DI	`00884838086982`
Brand	Flexible Module Server FMX-4
Model	Flexible Module Server FMX-4
Catalog no.	866468
Company	Philips Medizin Systeme Böblingen GmbH
Product code	MHX · Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	MR Unsafe
Status	In Commercial Distribution
Record updated	Dec 20, 2024

Device type (GMDN): Patient monitoring system module rack

A device typically designed as a framework or specially constructed holder where module devices used with a patient monitoring system can be plugged in and connected to the parent device usually by one cable. This device is typically used to facilitate connection to the patient from the modules using standard length cables and leads when the parent device is situated away from the patient (out of reach), e.g., the parent device may be mounted to a wall support or a ceiling pendant arm (Utility supply system).

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All Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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