NMT Module IntelliVue NMT ModuleRecalls & reported problems
Philips Medizin Systeme Böblingen GmbH · IntelliVue NMT Module is a quantitative measurement of the level of muscle relaxation as a consistent part of the IntelliVue patient monitoring. · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00884838029583), received between Oct 8, 2020 and Oct 29, 2024 — classified as 3 injuries, 1 malfunction.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (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.
Reports received per month
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings2
- Failure to Calibrate1
- Overheating of Device1
- Patient Device Interaction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Blister1
- Burn(s)1
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryOct 29, 2024Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THE MEASUREMENT WAS UNRELIABLE AND THE ANESTHESIOLOGIST ADMINISTERED MEDICATION TO REVERSE PARALYTIC AGENTS. NO OTHER CLINICAL INFORMATION OR MEDICAL INTERVENTION WAS REPORTED; THEREFORE, GOOD FAITH EFFORTS ARE ONGOING.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 20560247 ↗InjuryJan 4, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
THE CUSTOMER REPORTED THAT THE SYSTEM TRANSDUCER HAS HAD EXCESSIVE LEAKAGE CURRENT CAUSING INJURY TO THE PATIENT'S THUMB. THE DEVICE WAS IN USE AT THE TIME OF THE EVENT, THERE WAS AN INJURY TO THE PATIENT DURING THE EVENT REPORTED.
Patient problems: Blister
MAUDE report 18445604 ↗InjuryNov 6, 2023Overheating of Device; Overheating of Device
IT WAS REPORTED THE PATIENT DEVELOPED A BURN AT THE NMT ELECTRODE SITE, POSSIBLY FROM THE MODULE TEMPERATURE BEING SET TOO HIGH.
Patient problems: Burn(s)
MAUDE report 18074697 ↗MalfunctionOct 8, 2020Incorrect, Inadequate or Imprecise Result or Readings; Failure to Calibrate
THE CUSTOMER CALLED PHILIPS TO REPORT DIFFICULTIES WITH NMT MODULE CALIBRATION, AND IF THE MODULES DO CALIBRATE, INACCURATE READINGS HAVE BEEN OBSERVED. 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 10652658 ↗
Other STIMULATOR, NERVE, PERIPHERAL, ELECTRIC devices
- NMT cable IntelliVue NMT Patient CablePhilips Medizin Systeme Böblingen GmbH · STIMULATOR, NERVE, PERIPHERAL, ELECTRIC6 reports
- Smart Cable NMT Module and Accessories AF-201PNihon Kohden Corporation · Stimulator, Nerve, Peripheral, Electric1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.