HexaVue HexaVue IP (REF XQHPSLC)Recalls & reported problems
Black Diamond Video, Inc. · HexaVue IP Surgical Light Control Feature · Class 2
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00724995220587), received between Mar 5, 2026 and Jun 11, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (6 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.
Reports received per month
Most reported problems
Device problems
- Display or Visual Feedback Problem6
- No Display/Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 11, 2026Display or Visual Feedback Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THE IMAGE ON THE SURGICAL DISPLAY CONNECTED TO THEIR HEXAVUE IP CUSTOM ROOM RACK WAS "FLICKERING". THE PROCEDURE WAS COMPETED SUCCESSFULLY FOLLOWING A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25477135 ↗MalfunctionJun 11, 2026Display or Visual Feedback Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THE MONITORS CONNECTED TO THEIR HEXAVUE IP CUSTOM ROOM RACK WENT "BLACK" AND THE NURSE STATION MONITOR, MOUSE CONTROL AND TOUCHSCREEN WENT "BLACK". THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25477132 ↗MalfunctionMay 21, 2026No Display/Image
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE CAMERA BOX CONNECTED TO THEIR HEXAVUE IP CUSTOM ROOM RACK WOULD NOT DISPLAY VIDEO. THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25243224 ↗MalfunctionApr 24, 2026Display or Visual Feedback Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE TOUCH PANEL TO THEIR HEXAVUE IP CUSTOM ROOM RACK STOPPED RESPONDING RESULTING IN A PROCEDURE DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24985046 ↗MalfunctionMar 30, 2026Display or Visual Feedback Problem
THE USER FACILITY REPORTED THAT A MONITOR CONNECTED TO THEIR HEXAVUE IP CUSTOM ROOM RACK WOULD NOT DISPLAY PATIENT VITALS. THE EVENT DID NOT OCCUR DURING A PATIENT PROCEDURE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24713312 ↗MalfunctionMar 19, 2026Display or Visual Feedback Problem
THE USER FACILITY REPORTED THAT A MONITOR CONNECTED TO THEIR HEXAVUE IP CUSTOM ROOM RACK WOULD NOT DISPLAY AN IMAGE. THE EVENT DID NOT OCCUR DURING A PATIENT PROCEDURE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24643197 ↗MalfunctionMar 5, 2026Display or Visual Feedback Problem
THE USER FACILITY REPORTED THAT THE WALL MONITOR CONNECTED TO THEIR HEXAVUE IP CUSTOM ROOM RACK WAS UNABLE TO PRODUCE AN IMAGE. THE EVENT DID NOT OCCUR DURING A PATIENT PROCEDURE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24520795 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.