1788 1788210105Recalls & reported problems
Stryker Corporation · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 28
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 28 adverse event reports that list this exact device (DI 07613327580037), received between Jul 3, 2024 and Sep 30, 2026 — classified as 28 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (14 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/Image14
- Erratic or Intermittent Display6
- Poor Quality Image5
- Overheating of Device4
- Optical Problem2
- Output Problem2
- Application Program Problem1
- Connection Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions27
- Insufficient Information1
Recent adverse event reports
The 25 most recent of 28 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Erratic or Intermittent Display
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50955064 ↗MalfunctionSep 29, 2026Overheating of Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940526 ↗MalfunctionSep 18, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831243 ↗MalfunctionSep 11, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744579 ↗MalfunctionSep 11, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744510 ↗MalfunctionSep 10, 2026Erratic or Intermittent Display
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50725015 ↗MalfunctionSep 9, 2026Erratic or Intermittent Display
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50701507 ↗MalfunctionSep 2, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50576255 ↗MalfunctionSep 1, 2026No Display/Image
It was reported that when the camera cable is moved, the video image experiences interference and the video signal is lost. Therefore, there was loss of image.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50549691 ↗MalfunctionAug 13, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50245173 ↗MalfunctionAug 10, 2026Overheating of Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50194549 ↗MalfunctionAug 10, 2026Overheating of Device
It was reported that the camera system's functions cannot be controlled via the camera head, or can only be controlled with a significant delay. This leads to delays in surgery. In addition, the camera head becomes very hot due to these delays. This is particularly noticeable during a longer surgery.Therefore, there was a thermal event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50194205 ↗MalfunctionAug 3, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50124135 ↗MalfunctionJun 24, 2026No Display/Image; Output Problem
IT WAS REPORTED THAT WHEN THE CABLE IS MOVED, THE 1788 CAMERA IMAGE IS LOST. THE LOST OF IMAGE DURATION COULD NOT BE CONFIRMED, AND THE MEDICAL PROCEDURE WAS FINISHED WITH AN AUXILIARY/BACKUP DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25612159 ↗MalfunctionMay 11, 2026No Display/Image
IT WAS REPORTED THAT THE CAMERA HEAD IS DEFECTIVE AND THAT THE IMAGE SOMETIMES DISAPPEARS WHEN THE CABLE IS PULLED. THEREFORE, THERE WAS A LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25138085 ↗MalfunctionJan 21, 2026No Display/Image; Poor Quality Image
IT WAS REPORTED THAT THE MONITOR SCREEN FLICKERS REPEATEDLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24135194 ↗MalfunctionJan 12, 2026No Display/Image
IT WAS REPORTED THAT THE DEVICE WENT DOWN DURING A CASE. THERE WAS A DELAY OF LESS THAN 5 MINUTES FOR SWAPPING CAMERAS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24046531 ↗MalfunctionNov 21, 2025No Display/Image; Application Program Problem; No Display/Image; Application Program Problem
IT WAS REPORTED THAT WHEN USING THE CAMERA CONTROL UNIT DURING A PROCEDURE IT COMES ON THE SCREEN WITH E-03 ERROR AND TO TURN OFF.
Patient problems: Insufficient Information
MAUDE report 23619055 ↗MalfunctionAug 15, 2025Erratic or Intermittent Display; Erratic or Intermittent Display
IT WAS REPORTED THAT THE IMAGE WAS CUT OFF AND A REPLACEMENT WAS USED TO COMPLETE THE MEDICAL PROCEDURE. THEREFORE, THERE WAS PARTIAL IMAGE LOSS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22819796 ↗MalfunctionJul 28, 2025Erratic or Intermittent Display; Optical Problem; Erratic or Intermittent Display; Optical Problem
IT WAS REPORTED THAT THE IMAGE WAS CUT-OFF AND THAT A REPLACEMENT WAS USED TO COMPLETE THE MEDICAL PROCEDURE. THEREFORE, THERE WAS PARTIAL IMAGE LOSS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22636936 ↗MalfunctionJun 19, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THERE WAS IMAGE FAILURE AND LOOSE CONTACT DURING SURGERY. A REPLACEMENT WAS AVAILABLE TO BE USED TO COMPLETE THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22292251 ↗MalfunctionMay 12, 2025Overheating of Device; Temperature Problem; Overheating of Device; Temperature Problem
IT WAS REPORTED THAT STAFF SAID 1788 CAMERA BECAME SO HOT THEY WERE NOT ABLE TO HOLD IT. L12 LIGHT BOX WAS SET AT 50. STAFF USED A NEW CAMERA WITH NO ISSUES. 1788 CAMERA S/N (B)(6) WAS STILL HOT AFTER THE CASE ENDED. THEREFORE, THERE WAS A THERMAL EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22006458 ↗MalfunctionApr 28, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE DEVICE STOPPED WORKING DURING THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21919631 ↗MalfunctionFeb 24, 2025Erratic or Intermittent Display; Image Orientation Incorrect; Connection Problem; Erratic or Intermittent Display; Image Orientation Incorrect; Connection Problem
IT WAS REPORTED THAT THERE WAS INVERTED IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21453629 ↗MalfunctionDec 23, 2024Poor Quality Image; Optical Problem; Poor Quality Image; Optical Problem
IT WAS REPORTED THAT THERE WAS DARK IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21004600 ↗
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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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