GlideScope® Titanium LoPro T3Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00879123003164), received between Aug 19, 2025 and Aug 22, 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 22, 2025Display or Visual Feedback Problem; Poor Quality Image; Display or Visual Feedback Problem; Poor Quality Image

  A CUSTOMER REPORTED THAT DURING A PATIENT PROCEDURE, USING A GLIDESCOPE TITANIUM LOPRO T3 REUSABLE LARYNGOSCOPE, THE IMAGE WAS DISTORTED RESULTING IN THE USER BEING UNABLE TO VISUALIZE THE AIRWAY. THE PROCEDURE WAS COMPLETED USING A DIFFERENT LARYNGOSCOPE. NO DELAY IN PROCEDURE OR HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22873803 ↗
• MalfunctionAug 19, 2025Display or Visual Feedback Problem; Poor Quality Image; Display or Visual Feedback Problem; Poor Quality Image

  A FACILITY REPORTED THAT DURING AN ENDOTRACHEAL INTUBATION, USING A GLIDESCOPE TITANIUM LOPRO T3 REUSABLE LARYNGOSCOPE, THE IMAGE WAS SO POOR AND FUZZY/BLURRY THAT THE USER NEEDED TO COME BACK OUT OF THE PATIENT'S MOUTH TO APPLY ALCOHOL TO THE LENS IN ORDER TO IMPROVE THE IMAGE. IT WAS REPORTED THAT IT WAS NOT AN EMERGENCY SITUATION AND THE PATIENT WAS STABLE. NO DELAY IN PROCEDURE, USE OF A BACKUP DEVICE, OR HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22841687 ↗