ENDOCAM 5525108Recalls & reported problems
Richard Wolf GmbH · LOGIC HD CAMERA CONTROLLER touch screen, color display, compatible with core nova, Output: 2x HDMI, 2x 3G-SDI, 1x FBAS, 1x S-Video, Input: 1x 3G-SDI (PiP), Capturing video/images on USB, Resolution:1920x1200, U: 100-240VAC, 50/60Hz, Dim (wxhxd) 300x119,5x416mm · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04055207013212), received between Nov 27, 2019 and Nov 27, 2019 — classified as 1 malfunction.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Display or Visual Feedback Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 27, 2019Display or Visual Feedback Problem; Display or Visual Feedback Problem
ON OCTOBER 28, 2019, RICHARD WOLF GMBH (RW GMBH) RECEIVED THE FOLLOWING INFORMATION: DURING A PROCEDURE, THE CONTROLLER FROZE THE IMAGE DURING SURGERY. IMAGE FREEZE WAS CONTINUOUS. THE MALFUNCTION HAD OCCURED TWICE BEFORE AND WAS ABLE TO BE RESOLVED BY RESTARTING THE DEVICE. AFTER THE ERROR THE VIDEO MATERIAL WAS REPLACED BY ANOTHER BRAND AND THE SURGERY WAS CONTINUED. NO SIGNIFICANT DELAY. THE TREATMENT COULD BE COMPLETED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9386969 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.