IntelliBridge IntelliBridge EC40/80Recalls & reported problems
Philips Medical Systems Hsg · IntelliBridge EC40/80 · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00884838090811), received between Dec 23, 2021 and Sep 8, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Defective Alarm” (2 reports).
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
Most reported problems
Device problems
- Defective Alarm2
- Patient Data Problem2
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2025Defective Alarm; Defective Alarm
PHILIPS RECEIVED A COMPLAINT ON THE INTELLIBRIDGE EC40/80 INDICATING THERE WAS NO MORE TRANSMISSION OF ALARMS FROM THE FAN TO THE MONITOR. 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 22993498 ↗MalfunctionJul 2, 2025Defective Alarm; Defective Alarm
IT WAS REPORTED THAT THE INTELLIBRIDGE EC80 HUB IS NOT REPORTING VENTILATOR ALARMS TO THE CENTRAL 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 22383875 ↗MalfunctionAug 16, 2022Patient Data Problem; Patient Data Problem
THE CUSTOMER REPORTED THAT THE DATA OF TWO EC40 ARE ASSOCIATED WITH THE SAME PATIENT IN ICCA. ROOM 30 HAS THE PATIENT DATA FROM ROOM 36. THE DEVICE WAS IN USE ON A PATIENT. THERE WAS NO REPORT OF PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15237761 ↗MalfunctionJan 14, 2022Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
THE CUSTOMER REPORTED: : THE AUTO-CHARTING MADE THAT STRICTLY THE SAME DATA WERE TRANSFERRED TO THE INTELLISPACE CRITICAL CARE AND ANESTHESIA (ICCA), WHILE THIS VARIES ON THE RESPIRATOR (IN PARTICULAR FOR THE MEASURED DATA). SO INCORRECT DATA IN ICCA, AND THE DATA HAS TO BE CORRECTED MANUALLY, DESPITE THE BURDENSOME COVID SITUATION. THE DEVICE WAS REPORTED TO BE IN USE ON A PATIENT, BUT NO ADVERSE EVENT TO PATIENT OR USER WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13258280 ↗MalfunctionDec 23, 2021Patient Data Problem; Patient Data Problem
THE CUSTOMER REPORTED THAT THEIR SYSTEM WAS RECORDING INCORRECT VENTILATOR DATA. THE DEVICE WAS REPORTED TO BE IN USE ON A PATIENT, BUT NO ADVERSE EVENT TO PATIENT OR USER WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13079213 ↗
Other MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) devices
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- 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
- 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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