IntelliVue Multi Measurement Server SLCPRecalls & reported problems

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 00884838055094), received between Apr 2, 2021 and Aug 10, 2026 — classified as 10 malfunctions.

The most frequently reported specific device problem is “Failure to Sense” (5 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.

Most reported problems

Recent adverse event reports

The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 10, 2026Incorrect Measurement

  It was reported that the device is not reading ECG values correctly. 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 50191877 ↗
• MalfunctionDec 3, 2024Defective Alarm; Defective Alarm

  IT WAS REPORTED THE DEVICE DID NOT ALARM WHEN THE PATIENT HAD LOW PULSE OX. 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 20837469 ↗
• MalfunctionMay 4, 2023No Audible Prompt/Feedback; No Audible Prompt/Feedback

  THE CUSTOMER REPORTED A SPEAKER MALFUNCTION, IT IS UNKNOWN OF STILL SOUND WAS COMING FROM THE DEVICE. IT IS UNKNOWN IF THE DEVICE WAS NOT USE AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16868121 ↗
• MalfunctionJan 9, 2023Failure to Sense; Failure to Sense

  THE CUSTOMER REPORTED A NEONATAL DISPOSABLE BLOOD OXYGEN PROBE MEASUREMENT ERROR AFTER ONE HOUR OF MEASUREMENT; THE PROBE CAN'T MEASURE OXIMETRY (SPO2) AFTER ONE HOUR. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED. ON 22DEC2022, THE PHILIPS DISTRIBUTOR INVESTIGATING THE CASE FOUND THE SPO2 WAS LOST IN ISOLATION, AND THERE WERE NO ERROR MESSAGES OR ALARMS FROM OTHER PARAMETERS THAT ALERTED THE CLINICAL STAFF TO THE PROBLEM. THE DISTRIBUTOR CONFIRMED THE SPO2 SENSOR WAS FAULTY AND REPLACED THE SPO2 SENSOR. THE ISSUE WAS RESOLVED. THE DISTRIBUTOR ADVISED THE CUSTOMER TO ORDER A REPLACEMENT SENSOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16120145 ↗
• MalfunctionJan 6, 2023Failure to Sense; Failure to Sense

  THE CUSTOMER REPORTED A NEONATAL DISPOSABLE BLOOD OXYGEN PROBE MEASUREMENT ERROR AFTER ONE HOUR OF MEASUREMENT; THE PROBE CAN'T MEASURE OXIMETRY (SPO2) AFTER ONE HOUR. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED. ON 22DEC2022, THE PHILIPS DISTRIBUTOR INVESTIGATING THE CASE FOUND THE SPO2 WAS LOST IN ISOLATION, AND THERE WERE NO ERROR MESSAGES OR ALARMS FROM OTHER PARAMETERS THAT ALERTED THE CLINICAL STAFF TO THE PROBLEM. THE DISTRIBUTOR CONFIRMED THE SPO2 SENSOR WAS FAULTY AND REPLACED THE SPO2 SENSOR. THE ISSUE WAS RESOLVED. THE DISTRIBUTOR ADVISED THE CUSTOMER TO ORDER A REPLACEMENT SENSOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16117458 ↗
• MalfunctionJan 6, 2023Failure to Sense; Failure to Sense

  THE CUSTOMER REPORTED A NEONATAL DISPOSABLE BLOOD OXYGEN PROBE MEASUREMENT ERROR AFTER ONE HOUR OF MEASUREMENT; THE PROBE CAN'T MEASURE OXIMETRY (SPO2) AFTER ONE HOUR. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED. ON (B)(6) 2022, THE PHILIPS DISTRIBUTOR INVESTIGATING THE CASE FOUND THE SPO2 WAS LOST IN ISOLATION, AND THERE WERE NO ERROR MESSAGES OR ALARMS FROM OTHER PARAMETERS THAT ALERTED THE CLINICAL STAFF TO THE PROBLEM. THE DISTRIBUTOR CONFIRMED THE SPO2 SENSOR WAS FAULTY AND REPLACED THE SPO2 SENSOR. THE ISSUE WAS RESOLVED. THE DISTRIBUTOR ADVISED THE CUSTOMER TO ORDER A REPLACEMENT SENSOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16117407 ↗
• MalfunctionJan 6, 2023Failure to Sense; Failure to Sense

  THE CUSTOMER REPORTED A NEONATAL DISPOSABLE BLOOD OXYGEN PROBE MEASUREMENT ERROR AFTER ONE HOUR OF MEASUREMENT; THE PROBE CAN'T MEASURE OXIMETRY (SPO2) AFTER ONE HOUR. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED. ON (B)(6) 2022, THE PHILIPS DISTRIBUTOR INVESTIGATING THE CASE FOUND THE SPO2 WAS LOST IN ISOLATION AND THERE WERE NO ERROR MESSAGES OR ALARMS FROM OTHER PARAMETERS THAT ALERTED THE CLINICAL STAFF TO THE PROBLEM. THE DISTRIBUTOR CONFIRMED THE SPO2 SENSOR WAS FAULTY AND REPLACED THE SPO2 SENSOR. THE ISSUE WAS RESOLVED. THE DISTRIBUTOR ADVISED THE CUSTOMER TO ORDER A REPLACEMENT SENSOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16117406 ↗
• MalfunctionJan 6, 2023Failure to Sense; Failure to Sense

  THE CUSTOMER REPORTED A NEONATAL DISPOSABLE BLOOD OXYGEN PROBE MEASUREMENT ERROR AFTER ONE HOUR OF MEASUREMENT; THE PROBE CAN'T MEASURE OXIMETRY (SPO2) AFTER ONE HOUR. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED. ON 22DEC2022, THE PHILIPS DISTRIBUTOR INVESTIGATING THE CASE FOUND THE SPO2 WAS LOST IN ISOLATION, AND THERE WERE NO ERROR MESSAGES OR ALARMS FROM OTHER PARAMETERS THAT ALERTED THE CLINICAL STAFF TO THE PROBLEM. THE DISTRIBUTOR CONFIRMED THE SPO2 SENSOR WAS FAULTY AND REPLACED THE SPO2 SENSOR. THE ISSUE WAS RESOLVED. THE DISTRIBUTOR ADVISED THE CUSTOMER TO ORDER A REPLACEMENT SENSOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16111805 ↗
• MalfunctionDec 29, 2022No Audible Alarm; No Audible Alarm

  THE CUSTOMER REPORTED REPORTED THAT THE NEO SPO2 DISPOSABLE SENSOR FAILURE AFTER 1 HOUR OF MEASUREMENT. THE DEVICE WAS USED FOR PATIENT MONITORING AT THE TIME OF THE ALLEGED MALFUNCTION, THERE WAS NO ADVERSE EVENT REPORTED. A PHILIPS FIELD SERVICE ENGINEER (FSE) WENT TO THE CUSTOMER SITE. THE ENGINEER DETERMINED THAT THE ISSUES WAS ASSOCIATED WITH THE NEO SPO2 DISPOSABLE SENSOR. AFTER REPLACEMENT THE SPO2 SENSOR WAS RETURNED TO FUNCTIONAL USE WITH NO FURTHER ISSUE(S) IDENTIFIED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16066621 ↗
• MalfunctionApr 2, 2021Loss of Data; Loss of Data

  THE CUSTOMER REPORTED A LOSS OF SPO2 PARAMETER DATA WITH THEIR INTELLIVUE MULTI MEASUREMENT SERVER SLCP. IT IS 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 11608905 ↗