Expression IP5 Information Portal Expression Information Portal (IP5)Recalls & reported problems
Philips Ds North America LLC · The Expression Information Portal is a non-MRI remote display and controller for wireless Philips and Invivo MRI Patient Monitoring systems. It can be used from the control room, induction, or recovery areas, for providing clinicians an enhanced monitoring, case management, and connectivity experience. The basic system consists of the 19" widescreen touch display, HL7 data output capability, and radio module. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 00884838031890), received between Feb 21, 2020 and Sep 25, 2026 — classified as 12 malfunctions.
The most frequently reported specific device problem is “No Audible Alarm” (3 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
- No Audible Alarm3
- No Audible Prompt/Feedback3
- Application Program Freezes or Fails to Launch2
- Detachment of Device or Device Component1
- Erratic or Intermittent Display1
- Incorrect Measurement1
- Unable to Obtain Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions10
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50903412 ↗MalfunctionApr 24, 2024No Audible Prompt/Feedback; No Audible Prompt/Feedback
PHILIPS RECEIVED A COMPLAINT ON THE EXPRESSION INFORMATION PORTAL INDICATING THAT THE UNIT HAS NO AUDIO. 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 19173057 ↗MalfunctionApr 10, 2024No Audible Alarm; No Audible Alarm
THE CUSTOMER REPORTED THAT THERE WAS NO SOUND IN THE QRS TONE ON THE IP5. THEY ADVISED THE TOUCHSCREEN DOES NOT BEEP WHEN TOUCHING AS WELL, AND ADVISED THAT QRS WAS SET TO OFF, BUT WHEN TURNED BACK ON THEY STILL HAD NO SOUND. PER THE CALLER, ALL THE ALARMS ARE SET TO VOLUME 10. 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 19078448 ↗MalfunctionFeb 17, 2022Erratic or Intermittent Display; Erratic or Intermittent Display
IT WAS REPORTED THAT SINCE LAST WEEK, THE CUSTOMER WAS REPORTING AN ISSUE WITH THE TOUCH SCREEN. IT WAS ALLEGED THAT INTERMITTENTLY, THE TOUCH SCREEN HANGS AND THE USER CANNOT PERFORM ANY TASK. THE ONLY OPTION WAS TO RESTART THE IP5. IT IS UNKNOWN IF THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE EVENT, NO ADVERSE EVENT OR PATIENT HARM WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13550944 ↗MalfunctionJan 24, 2022No Audible Alarm; No Audible Alarm
IT WAS REPORTED THAT THERE WAS NO ALARM SOUND OR QRS TONE. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13337869 ↗MalfunctionNov 2, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE MONITOR ENTERED THE MRI ROOM AND BROKE WHEN PULLED INTO IT. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12739362 ↗MalfunctionOct 6, 2021Application Program Freezes or Fails to Launch; Application Program Freezes or Fails to Launch
IT WAS REPORTED THAT THE TOUCH SCREEN ON THE COMPLAINT DEVICE LOCKED UP AND THAT THE SYSTEM DID NOT RESPOND. 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 12586689 ↗MalfunctionSep 22, 2021Incorrect Measurement; Incorrect Measurement
IT WAS REPORTED THAT THE COMPLAINT DEVICE MADE A SIREN-LIKE WAIL, THE POWER SHUT OFF AND THAT THE SOFTWARE WAS FROZEN. 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 12513597 ↗MalfunctionJul 29, 2021Unable to Obtain Readings; Unable to Obtain Readings
THE CUSTOMER REPORTED THAT THE DOCTOR CLAIMED THAT THE NIBP (NON-INVASIVE BLOOD PRESSURE) READINGS WERE NOT UPDATING ON THE IP5 DISPLAY (IN THE NBP SECTION) BUT THEY COULD SEE THE NBP READINGS WITHIN THE TREND MENU ON THE COMPLAINT DEVICE. THE COMPLAINT DEVICE WAS IN CLINICAL USE AT THE TIME THAT THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT, OR PATIENT HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12246608 ↗MalfunctionNov 2, 2020No Audible Prompt/Feedback
THE CUSTOMER REPORTED THAT THE DEVICE'S AUDIO WAS NOT WORKING. 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 10773662 ↗MalfunctionApr 24, 2020No Audible Prompt/Feedback
THE CUSTOMER CLAIMED THAT THE DEVICE LOST AUDIO SOUND. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Patient Involvement
MAUDE report 9995493 ↗MalfunctionFeb 21, 2020No Audible Alarm
THE CUSTOMER REPORTED THAT THE DEVICE IS NOT PRODUCING ANY AUDIO. THE DEVICE WAS IN USE ON A PATIENT. THERE WAS NO REPORT OF PATIENT OR USER HARM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9739026 ↗
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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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