1788 1788710105Recalls & reported problems
Stryker Corporation · 1788 4K Inline Camera Head, C-Mount · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327580082), received between Jul 24, 2025 and Sep 24, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Erratic or Intermittent Display” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Erratic or Intermittent Display2
- Optical Problem2
- No Display/Image1
- Overheating of Device1
- Poor Quality Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Poor Quality Image
It was reported that there was an unspecified issue with the picture. Therefore, there was a poor image quality.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50888688 ↗MalfunctionSep 16, 2026No Display/Image
It was reported that the image was cycling through white balance, video loading, and the displayed video on the monitor. The video issue was resolved as soon as the camera was replaced. Therefore, there was a full loss of image.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794840 ↗MalfunctionSep 2, 2026Overheating of Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50576254 ↗MalfunctionJul 24, 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 22595532 ↗MalfunctionJul 24, 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 22595531 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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