CONMED IM8120Recalls & reported problems
Conmed Corporation · TRUE HD 3MOS CAMERA HEAD - EYECUP · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854080610), received between Oct 1, 2019 and Oct 1, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (1 report).
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.
Most reported problems
Device problems
- Display or Visual Feedback Problem1
- Loose or Intermittent Connection1
Patient problems
- Patient Problem/Medical Problem1
- Perforation of Vessels1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 1, 2019Display or Visual Feedback Problem; Loose or Intermittent Connection; Display or Visual Feedback Problem; Loose or Intermittent Connection
THE CONMED REPRESENTATIVE REPORTED ON BEHALF OF THE FACILITY THAT THE IM8120, TRUE HD CAMERA HEAD, DURING A GALLBLADDER PROCEDURE ON (B)(6) 2019 WENT DARK DUE TO INTERFERENCE WITH THE VALLEY LAB AND COVIDIEN UNITS. THE LOSS OF VISION CAUSED THE PATIENTS' BLOOD VESSEL TO BE CUT. THE PATIENT WAS TAKEN POST PROCEDURE TO THE EMERGENCY ROOM. THERE IS NO FURTHER INFORMATION ON THE PATIENT STATUS. THIS REPORT IS BEING RAISED DUE TO PATIENT INJURY.
Patient problems: Patient Problem/Medical Problem; Perforation of Vessels
MAUDE report 9140810 ↗
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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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