EEG Module IntelliVue EEG ModuleRecalls & reported problems
Philips Medizin Systeme Böblingen GmbH · IntelliVue EEG Module M1027B for use with IntelliVue Patient Monitors MP40-MP90 and MX500-MX800. The module provides continuous real-time monitoring of the Electroencephalogram (EEG) and produces four channels of EEG waveforms with Compressed Spectral Array (CSA) analysis. · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838031999), received between Sep 27, 2026 and Sep 27, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Output Problem” (1 report).
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
- Output Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 27, 2026Output Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50910006 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.