IntelliVue G7m Gas Analyzer Module IntelliVue G7m Anesthesia Gas ModuleRecalls & reported problems
Philips Medizin Systeme Böblingen GmbH · IntelliVue G7m Anesthesia Gas Module for use with IntelliVue MP40 to MP90 and MX500/550/600/700/800 monitors · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884838051492), received between Mar 28, 2018 and Oct 23, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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.
Reports received per month
Recalls naming this device
- Jan 18, 2023Class IIOpen, Classified
The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component issue that may trigger an interruption of the gas measurement. This issue concerns the G7m's sample gas pump which could stop working, producing a technical, INOP (inoperable) alarm. The pump may fail prematurely when there is friction caused by an abrasion. This recall is for an IMPORTANT PRODUCT NOTICE dated 1/18/23.
Z-0007-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Device Operates Differently Than Expected1
- Low Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 23, 2025Low Readings; Low Readings
IT WAS REPORTED THE BIOMED WAS PERFORMING PREVENTATIVE MAINTENANCE AND IDENTIFIED THE O2 LEVEL IS CONSTANTLY READING LOW. THE DEVICE WAS NOT IN USE ON A PATIENT AT THE TIME OF THE EVENT, THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23368975 ↗MalfunctionMar 28, 2018Device Operates Differently Than Expected
THE CUSTOMER REPORTED THAT HE USED THE INTELLIVUE G7M ANESTHESIA GAS MODULE DURING A CASE AND THEY HAD MISSING CO2 WAVE FORMS. THERE WAS NO INDICATION OF ANY HEALTH IMPACT TO A PATIENT AT ANY TIME. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE (LOSS OF C02 WAVE) WAS DISCOVERED. BUT THERE WAS NO USER OR PATIENT HARMED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7377878 ↗
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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