IntelliVue DockRecalls & reported problems
Philips Medizin Systeme Böblingen GmbH · IntelliVue Dock. Docking solution for X3 and MX100 monitors, providing mounting, AC power, LAN, and Flexible Sync Out. To be used with standalone IntelliVue X3 or IntelliVue MX100 monitors. Includes Universal Clamp and Cable Management Hook. Note that IntelliVue Dock cannot be used for connecting IntelliVue X3 to an IntelliVue host monitor. · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884838085244), received between Feb 11, 2019 and Aug 17, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Fell” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Device Fell2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 17, 2021Device Fell; Device Fell
THE CUSTOMER REPORTED THAT THE POOR DESIGN OF INTELLIVUE DOCK - MONITOR FELL AND HIT A PATIENTS HEAD - NO HARM TO PATIENT WAS REPORTED. THE DEVICE WAS USED FOR PATIENT MONITORING AT THE TIME OF THE ALLEGED MALFUNCTION. NO ADVERSE EVENT INVOLVING PATIENT OR USER WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12332256 ↗MalfunctionFeb 11, 2019Device Fell
THE CUSTOMER REPORTED THAT THE "X3 FELL OFF A MOUNT AND HIT A PATIENT ON THE HEAD. NO ADVERSE EVENT INVOLVING PATIENT OR USER WAS REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8324849 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.