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PANOVIEW 8654431Recalls & reported problems

Richard Wolf GmbH · TELESCOPE 12° Ø 4MM WL 297MM rigid, TL 363mm, rod lens system · 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 04055207018804), received between May 27, 2021 and May 27, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Optical Distortion” (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

  • Optical Distortion1
  • Poor Quality Image1

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.

  • MalfunctionMay 27, 2021Poor Quality Image; Optical Distortion; Poor Quality Image; Optical Distortion

    SEE MANUFACTURERS NARRATIVE FOR RESULTS OF THE DEVICE INVESTIGATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11895248 ↗

Other ENDOSCOPE, RIGID devices

All ENDOSCOPE, RIGID devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.