Capnography extension 862187Recalls & reported problems
Philips Medizin Systeme Böblingen GmbH · Capnography Extension works together with the IntelliVue Multi-Measurement Module (MMS), the IntelliVue X2 Multi-Measurement Module and IntelliVue MP2 Patient Monitor. The base product provides CO2 waveform, inspired minimum (imCO2), endtidal CO2 (etCO2) and Airway Respiration Rate (awRR) of intubated and non-intubated adult, pediatric and neonatal patients varies care areas inside the hospital. Optional Invasive Pressure, Temperature Cardiac Output (C.O.) and Continuous C.O. PiCCO can be selected via C-options. · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838021549), received between Nov 17, 2021 and Nov 17, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Device Fell” (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.
Most reported problems
Device problems
- Device Fell1
Patient problems
- Head Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 17, 2021Device Fell; Device Fell
IT WAS REPORTED THAT A MULTIMEASUREMENT SERVER (MMS) WAS ATTACHED TO A CAPNOGRAPHY EXTENSION. BOTH WERE USED IN COMPANION MODE WITH A INTELLIVUE MX700 PATIENT MONITOR. DURING USE THE MMS WAS SEPARATED FROM THE CAPNOGRAPHY EXTENSION AND FELL ON THE PATIENT'S HEAD. THE MMS FELL ON PATIENT'S HEAD. THE PATIENT UNDERWENT A CT SCAN OF THE HEAD.
Patient problems: Head Injury
MAUDE report 12832209 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.