IntelliVue Multi Measurement Server X2 865039Recalls & reported problems

Summary

The FDA's MAUDE database contains 506 adverse event reports that list this exact device (DI 00884838000261), received between Feb 23, 2018 and Sep 29, 2026 — classified as 7 deaths, 14 injuries, 485 malfunctions.

The most frequently reported specific device problem is “No Audible Alarm” (215 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.

Recalls naming this device

1. Oct 31, 2025Class IIOpen, Classified

   Potential issue where the IntelliVue monitors did not alarm.

   Z-0859-2026 · Root cause: Use error · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 506 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026No Audible Alarm

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50931438 ↗
• MalfunctionSep 15, 2026Incorrect Measurement

  Philips received a complaint on an IntelliVue Multi Measurement Server X2 indicating that SpO2 measurements could not be obtained and there is a suspicion that the SpO2 measurement was inaccurate. During remote troubleshooting replacement of the sensor cable did not resolve the issue. The device was reported to be in clinical use but not in use on a patient. No adverse event to the patient or user was reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50777524 ↗
• MalfunctionSep 3, 2026No Audible Prompt/Feedback

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50600077 ↗
• MalfunctionAug 12, 2026No Audible Prompt/Feedback

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50226107 ↗
• MalfunctionJun 30, 2026Imprecise or Erratic Results

  PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THEY WERE GETTING AN INCORRECT ARTERIAL READING. THE DEVICE WAS NOT IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE OR HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25670232 ↗
• MalfunctionApr 17, 2026Low Readings

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THE HEART RATE WAS SHOWING SLOW AND ABNORMAL. 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 24915913 ↗
• MalfunctionApr 14, 2026Incorrect Measurement

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THE ARTERIAL BLOOD PRESSURE PERFORMANCE TESTS SHOWED VALUES OUTSIDE THE SPECIFIED RANGE. 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 24879856 ↗
• MalfunctionApr 1, 2026Incorrect Measurement; Incorrect, Inadequate or Imprecise Result or Readings

  IT WAS REPORTED THAT NON-INVASIVE BLOOD PRESSURE (NIBP) VALUES WERE OUTSIDE THE SPECIFIED VALUE RANGE. IT IS UNKNOWN IF 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 24754716 ↗
• MalfunctionMar 10, 2026Device Fell

  IT WAS REPORTED THAT THE GCX ARM BROKE OFF AND THE X2 FELL OFF AND HIT THE FLOOR. 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 24560487 ↗
• MalfunctionFeb 16, 2026No Audible Prompt/Feedback

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THEY REQUIRE SPARE SPEAKER. IT IS UNKNOWN IF THE DEVICE COULD PRODUCE AN AUDIBLE SOUND. 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 24349369 ↗
• MalfunctionJan 14, 2026No Audible Alarm

  IT WAS REPORTED THAT A SPEAKER MALFUNCTION OCCURRED AND THE SPEAKER EMITS NO SOUND. 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 24068027 ↗
• InjuryJan 7, 2026Delayed Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THE DESATURATION (DESAT) LIMIT WAS SET TO 70%, AND IT TOOK 15-20 SECONDS BEFORE THE MONITOR ALARMED FOR DESAT WHEN THE PATIENT'S SATURATION WAS AT 35%.

  Patient problems: Low Oxygen Saturation

  MAUDE report 23992977 ↗
• MalfunctionJan 7, 2026No Audible Alarm

  PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THE SPEAKER WAS NOT WORKING; THERE WAS NO AUDIO ALARM. 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 23991011 ↗
• MalfunctionDec 30, 2025Imprecise or Erratic Results; Imprecise or Erratic Results

  PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THE NON-INVASIVE BLOOD PRESSURE MEASUREMENT VALUES WERE UNSTABLE. IT WAS UNKNOWN IF 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 23923078 ↗
• MalfunctionDec 20, 2025Defective Alarm; Defective Alarm

  THE CUSTOMER REPORTED AN ALARM ISSUE. THE DEVICE WAS NOT IN USE ON A PATIENT AT THE TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23858446 ↗
• MalfunctionDec 19, 2025No Audible Alarm; No Audible Alarm

  THE CUSTOMER REPORTED THERE WAS A BROKEN SPEAKER. IT WAS CONFIRMED THERE WAS NO AUDIO COMING FROM THE UNIT. THE DEVICE WAS NOT IN USE ON A PATIENT AT THE TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23847542 ↗
• MalfunctionDec 15, 2025Imprecise or Erratic Results; Imprecise or Erratic Results

  THE CUSTOMER REPORTED THAT NBP VALUE IS STRANGE. 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 23804495 ↗
• MalfunctionDec 9, 2025No Audible Alarm; No Audible Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THE SPEAKER WAS DEFECTIVE. THERE WAS NO SOUND. 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 23763090 ↗
• MalfunctionNov 25, 2025No Audible Alarm; No Audible Alarm

  THE CUSTOMER REPORTED A SPEAKER MALFUNCTION ERROR MESSAGE AND NO SOUND AFTER COMING BACK FROM BENCH REPAIR. THE DEVICE WAS IN CLINICAL 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 23646578 ↗
• MalfunctionNov 24, 2025No Audible Alarm; No Audible Prompt/Feedback; No Audible Alarm; No Audible Prompt/Feedback

  THE CUSTOMER REPORTED THAT SPEAKER IS DEFECTIVE. 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 23632957 ↗
• MalfunctionNov 10, 2025No Audible Alarm; No Audible Alarm

  IT WAS REPORTED THE DEVICE WAS PRESENTED WITH A SPEAKER MALFUNCTION ERROR MESSAGE AND THERE WAS NO SOUND COMING FROM THE DEVICE. THE DEVICE WAS NOT IN USE ON A PATIENT. THERE WAS NO REPORT OF PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23511087 ↗
• MalfunctionNov 3, 2025No Audible Alarm; No Audible Alarm

  PHILIPS RECEIVED A COMPLAINT ON INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT WHILE PERFORMING PRODUCT TRAINING, A SPEAKER EQUIPMENT MALFUNCTION INOP WAS DISPLAYED AND THERE WAS NO AUDIBLE SOUND WHEN THE DEVICE WAS TURNED ON. 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 23450639 ↗
• MalfunctionOct 22, 2025No Audible Alarm; No Audible Alarm

  IT WAS REPORTED THERE WAS A SPEAKER MALFUNCTION ERROR SHOWN ON THE SCREEN. IT WAS CONFIRMED AUDIO WAS NOT PRESENT AT THE TIME OF THE EVENT. THE DEVICE WAS IN USE ON A PATIENT AT THE TIME OF THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23360421 ↗
• MalfunctionOct 21, 2025Unable to Obtain Readings; Unable to Obtain Readings

  IT WAS REPORTED THAT THE DEVICE COULD NOT MEASURE SPO2 AND THERE WAS NO CONFIRMED INOP ERROR MESSAGE DISPLAYED. 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 23347076 ↗
• MalfunctionSep 2, 2025No Audible Alarm; No Audible Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER X2 INDICATING THAT THE DEVICE DISPLAYS A SPEAKER MALFUNCTION INOP ERROR MESSAGE AND DOES NOT EMIT AUDIBLE SOUND. THE DEVICE WAS NOT IN USE ON A PATIENT AT THE TIME OF THE EVENT, THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22931279 ↗