GlideScope® GlideScope® Core™ 10 FHDRecalls & reported problems
Verathon Medical (Canada) ULC · GlideScope® Core™ 10 FHD Monitor · Class 1
All models of GlideScope (36)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00879123008589), received between Sep 24, 2024 and Sep 8, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (3 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.
Reports received per month
Most reported problems
Device problems
- Display or Visual Feedback Problem3
- Erratic or Intermittent Display3
- Poor Quality Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2026Erratic or Intermittent Display; Display or Visual Feedback Problem; Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50674949 ↗MalfunctionJun 26, 2026Erratic or Intermittent Display; Display or Visual Feedback Problem
A CUSTOMER REPORTED WHILE USING A GLIDESCOPE CORE 10-INCH FHD MONITOR DURING A PATIENT INTUBATION, THE SCREEN WENT WHITE TWICE. A BACKUP DEVICE WAS USED TO COMPLETE THE PROCEDURE. NO PROCEDURAL DELAY OR PATIENT HARM WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25636140 ↗MalfunctionSep 24, 2024Erratic or Intermittent Display; Display or Visual Feedback Problem; Erratic or Intermittent Display; Display or Visual Feedback Problem
A CUSTOMER REPORTED THAT DURING INTUBATION OF A PATIENT, USING A GLIDESCOPE CORE 10-INCH FHD MONITOR, THE SCREEN WAS FLICKERING AND TURNED BLACK INTERMITTENTLY. THE PROCEDURE WAS COMPLETED BY USING THE SAME MONITOR BUT THEY REPORTED JIGGLING THE CABLE UNTIL A CLEAR PICTURE WAS OBSERVED. NO DELAY IN THE PROCEDURE, USE OF A BACKUP DEVICE, OR HARM TO THE PATIENT WAS REPORTED. FOLLOWING THE REPORTED EVENT, THE CUSTOMER'S VERATHON TERRITORY MANAGER EVALUATED THE SYSTEM AT THE FACILITY AND ISOLATED THE ISSUE TO THE MONITOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20292115 ↗
Other Laryngoscope, Rigid devices
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- McGRATH MAC 300-000-000Covidien LP · LARYNGOSCOPE, RIGID1 recall1 death205 reports
- n.a. 8404HXKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID242 reports
- McGRATH 340-000-000Covidien LP · LARYNGOSCOPE, RIGID2 deaths192 reports
- McGRATH MAC 301-000-000Covidien LP · LARYNGOSCOPE, RIGID2 recalls90 reports
- n.a. 8404BXCKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID141 reports
- n/a 8404AXCKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID108 reports
- McGRATH 340-000-000Covidien LP · LARYNGOSCOPE, RIGID84 reports
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
- 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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