IntelliVue Multi Measurement ServerRecalls & reported problems

Summary

The FDA's MAUDE database contains 28 adverse event reports that list this exact device (DI 00884838000254), received between Dec 18, 2018 and Aug 3, 2026 — classified as 2 deaths, 26 malfunctions.

The most frequently reported specific device problem is “Defective Alarm” (6 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 16, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 28 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 3, 2026Incorrect Measurement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50116697 ↗
• MalfunctionMar 23, 2026Incorrect Measurement

  IT WAS REPORTED THE IBP MEASUREMENT IS NOT READING ACCURATELY. THE DEVICE WAS IN CLINICAL USE. THERE WAS NO REPORT OF PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24663460 ↗
• MalfunctionFeb 13, 2026Incorrect Measurement

  IT WAS REPORTED THE DEVICE GIVES INACCURATE BLOOD PRESSURE (NIBP) MEASUREMENTS. THE DEVICE WAS IN CLINICAL USE. THERE WAS NO REPORT OF PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24330956 ↗
• MalfunctionFeb 10, 2026No Device Output

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER (MMS) INDICATING THAT THERE WAS A BLOOD OXYGEN (SPO2) FAILURE AND NO ERROR CODE FOUND. THE DEVICE WAS NOT IN USE ON A PATIENT AT THE TIME OF THE EVENT, SO THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24310807 ↗
• MalfunctionJan 13, 2026Imprecise or Erratic Results

  PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MULTI MEASUREMENT SERVER INDICATING THAT NON-INVASIVE BLOOD PRESSURE (NIBP) DYNAMIC HAD HIGHLY DIVERGENT VALUES. THE DEVICE WAS NOT IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24055330 ↗
• MalfunctionDec 9, 2025Failure to Deflate; Failure to Deflate

  IT WAS REPORTED THE BLOOD PRESSURE UNIT KEEPS INFLATING PRESSURE. 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 23754682 ↗
• MalfunctionMay 5, 2025Defective Alarm; Defective Alarm

  PHILIPS RECEIVED A COMPLAINT ON AN M3001A INTELLIVUE MULTI MEASUREMENT SERVER INDICATING THAT THERE WAS NO SPO2 MEASUREMENT, AND NO TECHNICAL ALARM MESSAGE DISPLAYED ON THE MONITOR. THE DEVICE WAS NOT IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. NO ADVERSE EVENT OR HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21962873 ↗
• MalfunctionApr 30, 2025Defective Alarm; Defective Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER INDICATING THERE WAS NO TECHNICAL ALARM. IT IS UNKNOWN IF THE DEVICE WAS 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 21935705 ↗
• MalfunctionJan 31, 2024Defective Alarm; Defective Alarm

  THE MODULE DISPLAYS YELLOW ALARMS INSTEAD OF RED ALARMS. 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 18613034 ↗
• MalfunctionOct 30, 2023Defective Alarm; Defective Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER INDICATING THE CUSTOMER EXPECTED AN ALARM TO SOUND FOR DESATURATION VALUE BEFORE 70. THE NURSE IN CHARGE OF THE BABY DID NOT HEAR AN ALARM SOUND FOR THE SPO2 VALUE WITNESSED. THE DEVICE WAS IN USE MONITORING A PATIENT AT THE TIME OF THE EVENT, THERE WAS NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18032408 ↗
• MalfunctionJun 12, 2023No Device Output; No Device Output

  THE CUSTOMER REPORTED THE SPO2 CUTS OUT. THE DEVICE WAS IN USE AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17109978 ↗
• MalfunctionApr 19, 2023High Readings; High Readings

  THE CUSTOMER REPORTED THAT THE INTELLIVUE MULTI MEASUREMENT SERVER PROVIDED SPO2 READINGS THAT WERE INACCURATELY HIGH FOR A VENTILATED PATIENT. THE DEVICE WAS IN USE MONITORING A PATIENT AT THE TIME OF THE REPORTED ISSUE. NO DEATH OR PATIENT / USER INJURY OR HARM WAS REPORTED.

  Patient problems: Hypoxia; No Clinical Signs, Symptoms or Conditions

  MAUDE report 16767718 ↗
• MalfunctionMar 7, 2023Incorrect Measurement; Incorrect Measurement

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MULTI MEASUREMENT SERVER SN (B)(6) INDICATING THE SP02 MEASUREMENT DID NOT MATCH AT ALL WITH THE MOCK MONITOR OR THE OTHER MONITOR IN THE ROOM DESPITE THE SP02 SENSOR BEING REPLACED. 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 16494870 ↗
• MalfunctionJan 19, 2023Defective Alarm; Defective Alarm

  IT WAS REPORTED THAT THE INTELLIVUE MULTI MEASUREMENT SERVER WAS UNABLE TO GENERATE AN APNEA ALARM. 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 16204600 ↗
• MalfunctionSep 12, 2022Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  IT WAS REPORTED THAT THE INTELLIVUE MULTI MEASUREMENT SERVER (MMS) HAD A SPO2 MALFUNCTION. THE MMS DISCONNECTED ITSELF FROM THE MONITOR. THE DEVICE WAS IN USE AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15406958 ↗
• MalfunctionJun 27, 2022Low Readings; Low Readings

  IT WAS REPORTED THAT THE SPO2 NUMERIC DID NOT GO ABOVE 60. 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 14836298 ↗
• MalfunctionApr 25, 2022No Audible Prompt/Feedback; No Audible Prompt/Feedback

  IT WAS REPORTED THAT THE DEVICE DOES NOT WORK ANYMORE, DOES NOT DIFFUSE THE ALARMS. THE DEVICE WAS NOT IN USE ON A PATIENT AT THE TIME OF THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14195133 ↗
• MalfunctionMar 28, 2022Defective Alarm; Defective Alarm

  IT WAS REPORTED THAT THE OXYGEN LEVEL FAILED TO A LEVEL OF 38%-60% AND THE DEVICE NEVER ALARMED. 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 13929236 ↗
• MalfunctionSep 29, 2021Intermittent Communication Failure; Intermittent Communication Failure

  IT WAS REPORTED THAT THE SATURATION INTERMITTENTLY DISAPPEARS WITHOUT AN ALARM MESSAGE TO REPORT IT. IT IS UNKNOWN IF THE DEVICE WAS IN CLINICAL USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12547525 ↗
• MalfunctionSep 7, 2021Low Readings; Low Readings

  THE CUSTOMER REPORTED THAT THE SPO2 SATURATION WAS NOT DISPLAYED CORRECTLY BY THE INTELLIVUE MULTI MEASUREMENT SERVER. THE DEVICE GAVE LOW VALUES. THE DEVICE WAS NOT IN USE ON A PATIENT AT THE TIME OF THE REPORTED ISSUE. NO DEATH, OR PATIENT/USER INJURY OR HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12436026 ↗
• MalfunctionJun 25, 2021Unable to Obtain Readings; Unable to Obtain Readings

  THE CUSTOMER REPORTED THERE WAS A DISCREPANCY BETWEEN TRACE CARRIED OUT WITH PHILIPS MONITORING 12-LEAD ECG AND THE ELECTROCARDIOGRAPH.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 12066142 ↗
• MalfunctionMay 5, 2021Audible Prompt/Feedback Problem; Audible Prompt/Feedback Problem

  THE CUSTOMER REPORTED THEIR INTELLIVUE MULTI MEASUREMENT SERVER (MMS) PRODUCED A DELAYED ALARM FOR A DESATURATION EVENT. 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 11777979 ↗
• MalfunctionApr 22, 2021No Audible Prompt/Feedback; No Audible Prompt/Feedback

  THE CUSTOMER REPORTED THEIR INTELLIVUE MULTI MEASUREMENT SERVER (MSS) DID NOT ALARM DURING A DESATURATION EVENT ON (B)(6) 2021. 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 11705850 ↗
• MalfunctionApr 20, 2020Device Alarm System; Device Displays Incorrect Message

  THE CUSTOMER REPORTED THAT THEIR DEVICE WAS NOT ALARMING CORRECTLY AND REGULARLY DISPLAYS AN X. THE DEVICE WAS REPORTED TO BE IN USE ON A PATIENT, BUT NO ADVERSE EVENT TO PATIENT OR USER WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9978261 ↗
• MalfunctionMar 27, 2020Intermittent Continuity

  THE CUSTOMER REPORTED THE SPO2 PARAMETER IS INTERMITTENTLY OPERATING ON THEIR INTELLIVUE MEASUREMENT SERVER (MMS) DEVICE. NO ADVERSE EVENT INVOLVING PATIENT OR USER WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9888601 ↗