GlideScope® Spectrum QC Miller S1Recalls & reported problems
Verathon Medical (Canada) ULC · GlideScope® Spectrum QC Miller S1 · Class 1
All models of GlideScope (36)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00879123007971), received between Feb 18, 2025 and Mar 18, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (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. 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 Problem2
- No Display/Image2
Patient problems
- Low Oxygen Saturation1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 18, 2025No Display/Image; Display or Visual Feedback Problem; No Display/Image; Display or Visual Feedback Problem
A CUSTOMER REPORTED THAT DURING A ROUTINE PATIENT INTUBATION, USING A GLIDESCOPE SPECTRUM SINGLE-USE QC MILLER S1 LARYNGOSCOPE, THE LIGHT SOURCE DID NOT WORK. IT WAS REPORTED THAT THE IMAGE WAS DARK UPON INSERTING THE BLADE INTO THE PATIENT'S MOUTH. SUBSEQUENTLY, THE DOCTOR OPTED TO COMPLETE THE INTUBATION VIA DIRECT LARYNGOSCOPY. NO DELAY IN THE PROCEDURE OR HARM TO THE PATIENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21634254 ↗MalfunctionFeb 18, 2025No Display/Image; Display or Visual Feedback Problem; No Display/Image; Display or Visual Feedback Problem
A CUSTOMER REPORTED THEY WERE ATTEMPTING TO INTUBATE A CHILD (UNKNOWN AGE) WITH A GLIDESCOPE SPECTRUM SINGLE-USE QC HYPERANGLE S2 LARYNGOSCOPE WITH A 4.5 MM ENDOTRACHEAL TUBE (ETT) AND A GLIDERITE STYLET (UNKNOWN SIZE OR MODEL). IT WAS REPORTED THAT THE LARYNGOSCOPE HAD A GREAT VIEW BUT THEY COULD NOT SEE TO SAFELY PASS THE ETT INTO THE OROPHARYNX AS BOTH THE LARYNGOSCOPE AND ETT COULD NOT FIT IN THE CHILD'S MOUTH. AFTER ATTEMPTING MINOR ADJUSTMENTS WITH THE C-COLLAR IN PLACE AND A DIFFERENT STYLET, THE PATIENT STARTED TO DESATURATE AT WHICH POINT THEY DECIDED TO MASK GENTLY AND THEN RETRY WITH A STRAIGHT BLADE. A GLIDESCOPE SPECTRUM SINGLE-USE QC MILLER S1 LARYNGOSCOPE WAS CONNECTED BUT WOULD NOT SHOW THE IMAGE. BOTH AVAILABLE CABLES WERE ATTEMPTED BUT STILL NO VIEW OR LIGHT DISPLAYED FROM THE LARYNGOSCOPE. THEY DECIDED TO REVERT BACK TO USING THE HYPERANGLE S2 LARYNGOSCOPE WHICH WAS INSERTED AT THE SAME TIME AS THE ETT, WITH REMOVAL OF THE FRONT OF THE C-COLLAR AND MANUAL IN-LINE STABILIZATION OF THE HEAD AND NECK. THE ETT WAS SAFELY PASSED THROUGH THE GLOTTIS. NO HARM TO THE PATIENT WAS REPORTED.
Patient problems: Low Oxygen Saturation
MAUDE report 21405006 ↗
Other Laryngoscope, Rigid devices
- McGRATH MAC 301-000-000Covidien LP · LARYNGOSCOPE, RIGID2 recalls202 reports
- 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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