L51KRecalls & reported problems
Fujifilm Corporation · Probe · Class 2
- 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 04573596212134), received between Mar 30, 2026 and Mar 30, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 30, 2026Use of Device Problem; Insufficient Device Problem Information
DURING THE SURGICAL PROCEDURE WITH A DA VINCI ROBOT, IN WHICH THE ULTRASOUND PROBE IS INSERTED INTO THE BODY THROUGH A TROCAR AND HOLD BY A GRASPING FORCEPS, PARTS OF THE CABLE SHEATH BROKE OFF. THERE WAS NO CLINICAL IMPACT ON THE PATIENT. THE DETACHED FRAGMENTS OF THE CABLE SHEATH WERE IMMEDIATELY VISUALIZED ON THE CAMERA DURING THE PROCEDURE AND REMOVED WITHOUT DIFFICULTY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24709785 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.