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HIGHLIGHT 5142002Recalls & reported problems

Richard Wolf GmbH · LIGHT SOURCE X 300 300W Xenon short arc lamp, dialog function, touch screen, color display, compatible with core nova, universal light cable connection, 6000K, U: 100-240VAC, 50/60Hz, Dim (wxhxd) 300x160x400mm · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 04055207012901), received between Mar 20, 2017 and Mar 20, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (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

  • Device Displays Incorrect Message1
  • Device Inoperable1

Patient problems

  • Patient Problem/Medical Problem1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 20, 2017Device Inoperable; Device Displays Incorrect Message; Device Inoperable; Device Displays Incorrect Message

    RICHARD WOLF (B)(4) WAS NOTIFIED THAT DURING A PROCEDURE THE DEVICE IN QUESTION STOPPED AND AN ERROR MESSAGE DISPLAYED ON SCREEN. A BACK UP DEVICE WAS NOT READILY AVAILABLE AND PROCEDURE STOPPED AND RESCHEDULED. DELAY IN PROCEDURE MAY HAVE PLACED PATIENT AT RISK.

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 6417335 ↗

Other Light source, endoscope, xenon arc devices

All Light source, endoscope, xenon arc devices →

Sources and updates

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