GlideScope® Video Baton QC LargeRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00879123007797), received between Aug 13, 2024 and Apr 29, 2025 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Display or Visual Feedback Problem” (5 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 29, 2025Erratic or Intermittent Display; Display or Visual Feedback Problem; Loose or Intermittent Connection; Erratic or Intermittent Display; Display or Visual Feedback Problem; Loose or Intermittent Connection

  A CUSTOMER REPORTED THAT DURING AN INTUBATION USING A GLIDESCOPE VIDEO BATON QUICKCONNECT LARGE, THE IMAGE WAS GOING IN AND OUT. FURTHERMORE, THE LIGHT FAILED TO ILLUMINATE CONSISTENTLY AND THE GLIDESCOPE CORE 2M QUICKCONNECT CABLE WAS NOT STAYING CONNECTED TO THE VIDEO BATON. THE PROCEDURE WAS COMPLETED USING A BACKUP DEVICE WHICH WAS MADE AVAILABLE IN AN UNSPECIFIED AMOUNT OF TIME. NO DELAY IN THE PROCEDURE OR HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21928738 ↗
• MalfunctionJan 14, 2025Crack; Display or Visual Feedback Problem; Poor Quality Image; Crack; Display or Visual Feedback Problem; Poor Quality Image

  A CUSTOMER REPORTED WHILE USING A GLIDESCOPE VIDEO BATON QUICKCONNECT LARGE DURING A PATIENT PROCEDURE, THERE WAS A CRACK IN THE MIDDLE OF THE CAMERA RESULTING IN A BIG, WHITE LINE AND USERS BEING UNABLE TO SEE. THE PROCEDURE WAS COMPLETED USING A BACKUP DEVICE WHICH WAS MADE AVAILABLE IN AN USPECIFIED AMOUNT OF TIME. NO DELAY IN THE PROCEDURE OR HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21152256 ↗
• MalfunctionOct 15, 2024Erratic or Intermittent Display; Display or Visual Feedback Problem; Erratic or Intermittent Display; Display or Visual Feedback Problem

  A CUSTOMER REPORTED WHILE USING A GLIDESCOPE VIDEO BATON QUICKCONNECT LARGE DURING A PATIENT PROCEDURE, THE LIGHT WAS FLASHING ON AND OFF AND INTERMITTENTLY DISPLAYING THE MESSAGE 'CAMERA NOT CONNECTED.' THE CUSTOMER TRIED SWAPPING THE VIDEO BATON FROM THE A PORT TO THE B PORT OF THE MONITOR BUT THE ISSUE PERSISTED. NO DELAY IN THE PROCEDURE, USE OF A BACKUP DEVICE, OR HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20457999 ↗
• MalfunctionSep 10, 2024Erratic or Intermittent Display; Display or Visual Feedback Problem; Erratic or Intermittent Display; Display or Visual Feedback Problem

  THE CUSTOMER REPORTED THAT DURING A PATIENT PROCEDURE, USING A GLIDESCOPE VIDEO BATON QUICKCONNECT LARGE, THE PICTURE ON THE CONNECTED GLIDESCOPE CORE 10-INCH MONITOR FREEZES WHEN THE GLIDESCOPE CORE QUICKCONNECT CABLE AND VIDEO BATON ARE MOVED. NO DELAY IN THE PROCEDURE, USE OF A BACKUP DEVICE, OR HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20182304 ↗
• MalfunctionAug 13, 2024No Display/Image; Display or Visual Feedback Problem; Poor Quality Image; No Display/Image; Display or Visual Feedback Problem; Poor Quality Image

  THE CUSTOMER REPORTED THAT DURING A PATIENT PROCEDURE, USING A GLIDESCOPE VIDEO BATON QUICKCONNECT LARGE, THE LIGHT WAS DIM WHEN TURNED ON; HOWEVER, THE SCREEN WENT BLACK ONCE THE VIDEO BATON WAS INSERTED INTO THE PATIENT'S AIRWAY. NO DELAY IN THE PROCEDURE, USE OF A BACKUP DEVICE, OR HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19973618 ↗