IntelliVue Patient Monitor MX750Recalls & reported problems
Philips Medizin Systeme Böblingen GmbH · The IntelliVue MX750 Patient Monitor has an optically-bonded 19 inch (469 mm) LCD (TFT) widescreen display with projected capacitive touch technology. It is compatible with various measurement modules and measurement servers. The monitor provides as standard a 100BaseT LAN port, an RS232 port, four USB ports, a basic nurse call relay, and an analog ECG sync output. MX750 also provides one MSL connector for connecting up to two FMX-4 module racks (in the case of two racks, the racks are connected to each other in series and then plugged in to the MSL connector). Built-in to the front of the display is a Contactless ID and Communication module using RFID technology. Please refer to technical data sheet for more information. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
Quick summary
This Philips IntelliVue patient monitor is a physiological monitor with arrhythmia detection and alarms. The 237 reports mostly describe monitors that did not sound alarms or prompts, along with alarm system problems and programs freezing. The reports include 21 injuries and 15 deaths, and some mention cardiac arrest or low oxygen levels in patients. There is 1 open recall, started in October 2025, over monitors that did not alarm.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 238
- Deaths reported
- 15
- Injuries reported
- 21
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 238 adverse event reports that list this exact device (DI 00884838083332), received between Aug 5, 2020 and Sep 30, 2026 — classified as 15 deaths, 21 injuries, 202 malfunctions.
The most frequently reported specific device problem is “No Audible Alarm” (107 reports).
1 FDA recall record name this device's identifier, 1 still open.
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 18, 2026.
Reports received per month
Recalls naming this device
- Oct 31, 2025Class IIOpen, Classified
Potential issue where the IntelliVue monitors did not alarm.
Z-0868-2026 · Root cause: Use error · Recall details · FDA record ↗
Most reported problems
Device problems
- No Audible Alarm107
- Defective Alarm44
- Device Alarm System25
- No Audible Prompt/Feedback22
- Incorrect Measurement8
- Application Program Freezes or Fails to Launch6
- Imprecise or Erratic Results4
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions205
- Insufficient Information16
- Cardiac Arrest10
- Low Oxygen Saturation7
- Low Blood Pressure/ Hypotension3
- Bradycardia2
- Tachycardia2
- Apnea1
Recent adverse event reports
The 25 most recent of 238 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026No Audible Alarm
Philips received a complaint on an IntelliVue MX750 Patient Monitor indicating that the device does not make sound alarm when connected to EVO ventilator. The device was in clinical use on a patient at the time of the event. No adverse event was reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950956 ↗MalfunctionSep 28, 2026Application Program Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923828 ↗MalfunctionSep 27, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50909970 ↗MalfunctionSep 22, 2026No Audible Alarm
Philips received a complaint on the IntelliVue MX750 Patient Monitor indicating that the speaker was defective. It was clarified that a speaker error was shown on the display, and no sound was audible. The device was in use on a patient at the time of the event. There was no adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50855676 ↗MalfunctionSep 22, 2026Low Readings
It was reported that during testing the diastolic pressure seems to be underestimated. The device was not in use on a patient at the time of the event. There was no adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50852582 ↗MalfunctionSep 18, 2026Device Alarm System
It was reported that the Alarms did not sound for a Bradycardia event. The device was in use on a patient at the time of the event. There was no adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50819029 ↗MalfunctionSep 18, 2026Device Alarm System
It was reported that the Alarms did not sound for an SPO2 event. The device was in use on a patient at the time of the event. There was no adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50818261 ↗MalfunctionSep 7, 2026Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50658749 ↗MalfunctionAug 27, 2026Application Program Problem
It was reported that the monitor has a different configuration than the rest on the station. The device was in use on a patient at the time of the event. There was no adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50470809 ↗InjuryAug 24, 2026Defective Alarm
Patient problems: Low Oxygen Saturation
MAUDE report 50410788 ↗MalfunctionJul 30, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50086745 ↗MalfunctionJul 17, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25852893 ↗MalfunctionJul 16, 2026No Audible Prompt/Feedback
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25850705 ↗MalfunctionJul 16, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25846425 ↗MalfunctionJul 14, 2026Defective Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25813995 ↗MalfunctionJul 14, 2026Incorrect Measurement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25812867 ↗MalfunctionJul 9, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25770542 ↗MalfunctionJul 7, 2026No Device Output
PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MX750 PATIENT MONITOR INDICATING THAT THE BEDSIDE MONITORS SPONTANEOUSLY LOST CUSTOM PROFILE FOR THIS UNIT. THE DEVICE WAS IN CLINICAL USE AT TIME OF EVENT, NO ADVERSE EVENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25733807 ↗MalfunctionJun 29, 2026Defective Alarm
PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MX750 PATIENT MONITOR INDICATING THAT THE PATIENT HAD A HEART RATE VTACH RED ALARM BUT THE MONITOR DID NOT GENERATE A VISUAL OR AUDIBLE ALARM. 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 25653766 ↗MalfunctionJun 22, 2026Delayed Alarm
PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MX750 PATIENT MONITOR INDICATING THAT THE NURSES ARE OBSERVING ALARM DELAYS ON THE SPO2 ALARMS. 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 25580406 ↗MalfunctionJun 18, 2026Incorrect Measurement
IT WAS REPORTED THE THE SPO2 VALUES HAVE FALSE AND DEVIATED VALUES. THE CUSTOMER USES SPO2 SENSORS FROM OTHER MANUFACTURERS. THE DEVICE WAS NOT IN CLINICAL USE. THERE WAS NO REPORT OF PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25546138 ↗MalfunctionMay 29, 2026No Audible Alarm
PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MX750 PATIENT MONITOR INDICATING THAT THE CUSTOMER WAS TRYING TO REPLACE THE SPEAKER AS THE MONITOR HAS NO SOUND AND NEEDED ASSISTANCE REPLACING THE SPEAKER. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25331407 ↗MalfunctionMay 18, 2026No Audible Alarm
CUSTOMER REPORTED THAT THE ¿SPEAKER MALFUNCTION¿ WAS DISPLAYED ON SCREEN, AND NO NOISE EMITTING DURING PATIENT MONITOR ALARM STATE CONFIRMING MACHINE FAULT. IT IS UNKNOWN IF THE DEVICE WAS IN WAS IN CLINICAL USE AT TIME OF EVENT, NO ADVERSE EVENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25208885 ↗MalfunctionMay 12, 2026Imprecise or Erratic Results
PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MX750 PATIENT MONITOR INDICATING THAT THE HEART RATE ON THE EKG IS VARYING BY A LARGE DEGREE COMPARED TO THE SPO2 HEART RATE. 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 25148993 ↗MalfunctionMay 12, 2026Incorrect Measurement
PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MX750 PATIENT MONITOR INDICATING THE NON-INVASIVE BLOOD PRESSURE (NIBP) MEASUREMENT IS INCORRECT. THIS DEVICE INDICATES A PRESSURE OF 47/50 WHEN THE VALUES FOR THE SAME PATIENT ARE NORMAL FOR ALL OTHER MONITORS. 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 25148228 ↗
Other Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) devices
- IntelliVue MX40 1.4GHz MX40 1.4 GHz Smart HoppingPhilips Medical Systems Hsg · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)1 recall47 deaths2,541 reports
- NA PU-621RNihon Kohden Corporation · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)17 deaths1,666 reports
- Tempus Pro 00-1024-RRemote Diagnostic Technologies Limited · Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)7 recalls8 deaths1,217 reports
- NA PU-681RANihon Kohden Corporation · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)22 deaths1,493 reports
- IntelliVue Multi-Measurement Module X3 IntelliVue X3Philips Medizin Systeme Böblingen GmbH · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)1 recall19 deaths1,172 reports
- Patient Information Center IXPhilips Medical Systems Hsg · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)82 deaths941 reports
- Patient Information Center iXPhilips Medical Systems Hsg · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)83 deaths814 reports
- Tempus Pro 00-1024-RRemote Diagnostic Technologies Limited · Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)5 recalls541 reports
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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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