32" 4K OLED Surgical Display 0240031300Recalls & reported problems
Stryker Corporation · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 07613327592146), received between Apr 17, 2023 and Sep 11, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (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. 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
- No Display/Image6
- Output Problem4
- Connection Problem1
- Device Fell1
- Electrical Power Problem1
- Temperature Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 11, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744581 ↗MalfunctionDec 5, 2025Device Fell; Device Fell
IT WAS REPORTED THAT OLED MONITOR CAME OFF ITS BACK PLATE AND FELL IN AN OR DURING SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23734896 ↗MalfunctionNov 25, 2025No Display/Image; Connection Problem; No Display/Image; Connection Problem
IT WAS REPORTED THAT THE DEVICE FAILED AND SHUT OFF IN THE MIDDLE OF A CASE CAUSING FULL LOSS OF IMAGE ON PRIMARY MONITOR. DURATION OF LOSS OF IMAGE WAS THAT IT NEVER CAME BACK ON. IT WAS FOR THE REMAINING PORTION OF THE CASE WHICH WAS APPROXIMATELY 60-90 MINUTE RANGE. PROCEDURE COMPLETED USING THE SECONDARY MONITOR. THERE WAS NO SURGICAL DELAY, IT WAS MORE ABOUT "PIVOTING" TO THE SECONDARY MONITOR TO COMPLETE THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23651038 ↗MalfunctionSep 30, 2025No Display/Image; No Display/Image
THE DEVICE IS THE PRIMARY MONITOR. THE OLED SCREEN TURNED WHITE AND WOULD NOT ROUTE TO A DIFFERENT SCREEN. THERE WAS AN IMAGE LOSS AND IT REMAINED LOST. THE IMAGE NEVER RETURNED AND THE CURRENT MONITOR IS NO LONGER USABLE. TO COMPLETE THE PROCEDURE, THERE WAS ANOTHER OLED HANGING IN THE ROOM, AND THE PROCEDURE WAS FINISHED WITH THAT MONITOR. THIS CAUSED A DELAY OF ABOUT 10 MINUTES
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23186996 ↗MalfunctionAug 13, 2025No Display/Image; Output Problem; No Display/Image; Output Problem
IT WAS REPORTED THAT DURING THE SURGERY, THE TOWER WAS FUNCTIONING NORMALLY WHEN SUDDENLY THE MONITOR TURNED OFF AND DID NOT DISPLAY AN IMAGE AT ANY TIME AFTERWARD. AFTER QUICKLY CHECKING POSSIBLE SOLUTIONS, THE MONITOR STILL DID NOT SHOW AN IMAGE, WHICH LED TO AN IMMEDIATE REPLACEMENT OF THE TOWER WITH ANOTHER UNIT PROVIDED BY THE CLIENT. NO ADVERSE EVENT OCCURRED, ALTHOUGH THE PROCEDURE TIME WAS EXTENDED DUE TO THE EQUIPMENT CHANGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22798159 ↗MalfunctionDec 22, 2023No Display/Image; Output Problem; No Display/Image; Output Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18387624 ↗MalfunctionDec 21, 2023No Display/Image; Output Problem; No Display/Image; Output Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18376401 ↗MalfunctionDec 13, 2023Electrical Power Problem; Temperature Problem; Electrical Power Problem; Temperature Problem
IT WAS REPORTED THAT THERE WAS A THERMAL EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18318715 ↗MalfunctionApr 17, 2023Output Problem; Output Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16753845 ↗
Other CAMERA, TELEVISION, SURGICAL, WITHOUT AUDIO devices
- VisionPro 0240031020Stryker Corporation · CAMERA, TELEVISION, SURGICAL, WITHOUT AUDIO16 reports
- Stryker 0240-031-050Barco, Inc. · Camera, Television, Surgical, Without Audio1 report
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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