IntelliBridge EC10 ModuleRecalls & reported problems
Philips Medizin Systeme Böblingen GmbH · The IntelliBridge EC10 module acquires real-time information from bedside devices e.g. mechanical ventilators, anesthesia machines, and multi-measurement devices for display on Philips IntelliVue patient monitors. · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00884838015951), received between Feb 21, 2020 and May 18, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Defective Alarm” (2 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Jan 15, 2025Open, Classified
Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.
Z-1106-2025 · Root cause: Software design · FDA record ↗
Most reported problems
Device problems
- Defective Alarm2
- Device Alarm System2
- Application Program Freezes or Fails to Launch1
- Incorrect Measurement1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 18, 2026Application Program Freezes or Fails to Launch
THE CUSTOMER REPORTED THAT THE DEVICE IS INTERMITTENTLY, AND THE VITALS COMING IN FREEZES AND DOES NOT CROSS OVER. 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 25211688 ↗MalfunctionSep 29, 2025Defective Alarm; Defective Alarm
IT WAS REPORTED THAT THE CUSTOMER IS USING INTELLIBRIDGE MODULES FOR DATA TRANSMISSION. SINCE HE RECENTLY PURCHASED CAPSULE E DEVICES TO DIGITIZE THE VENTILATION DATA HE IS NO LONGER RECEIVING ALARMS ON THE CONTROL CENTER VIA THE INTELLIBRIDGE MODULES. PATIENT INVOLVEMENT IS UNKNOWN. THERE WAS NO REPORT OF PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23166219 ↗MalfunctionDec 2, 2024Defective Alarm; Defective Alarm
PHILIPS RECEIVED A COMPLAINT ON THE INTELLIBRIDGE EC10 MODULE SYSTEM INDICATING AN UNSPECIFIC ALARM ISSUE. IT IS UNKNOWN IF THE DEVICE WAS NOT IN USE MONITORING A PATIENT AT THE TIME OF THE EVENT. NO ADVERSE EVENT INVOLVING A PATIENT OR USER WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20819319 ↗MalfunctionJan 31, 2023Device Alarm System; Device Alarm System
THE CUSTOMER REPORTED THAT AN ALARM GENERATED IN YELLOW ON A PRISMAX EQUIPMENT IS TRANSCRIBED IN BLUE ON AN MX750 MONITOR. THE CUSTOMER EXPECTS THE "DYLS EMPTY BAG" ALARM TO BE CONSIDERED AS A CRITICAL ALARM AND NOT A TECHNICAL ALARM. THE DEVICE WAS REPORTED TO BE IN USE ON A PATIENT, BUT NO ADVERSE EVENT TO THE PATIENT OR USER WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16270575 ↗MalfunctionDec 8, 2021Incorrect Measurement; Incorrect Measurement
IT WAS REPORTED THAT THE VALUE FOR THE INSPIRED TIME DISPLAYED ON THE INTELLIVUE MP70 PATIENT MONITOR WAS MUCH HIGHER THAN THE ACTUAL READING ON THE MAQUET SERVO-I VENTILATOR WHEN USING THE INTELLIBRIDGE EC10 MODULE. THE DEVICE WAS REPORTED TO BE IN USE ON A PATIENT, BUT NO ADVERSE EVENT TO THE PATIENT OR USER WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12960015 ↗MalfunctionFeb 21, 2020Device Alarm System
THE CUSTOMER REPORTED PROBLEMS WITH THE ALARM TRANSFER ON THEIR INTELLIBRIDGE EC10 MODULE. THERE WAS NO ADVERSE EVENT REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9738637 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.