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PANOVIEW PLUS 8965411Recalls & reported problems

Richard Wolf GmbH · NEPHROSCOPE 20° 24FR WL 224MM rigid, with lateral ocular lens, working channel for instruments up to 10.5Fr, TL 356mm, 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 04055207023327), received between May 29, 2018 and May 29, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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

  • Device Operates Differently Than Expected1
  • Poor Quality Image1

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.

  • MalfunctionMay 29, 2018Poor Quality Image; Device Operates Differently Than Expected; Poor Quality Image

    AT THE FIRST TEN MINUTES OF THE OPERATION THE NEPHROSCOPE 8965.411 WAS EXCELLENT AND THEN WE STARTED THE SECOND OPERATION AND VISION BEGAN TO DISAPPEAR GRADUALLY THE SAME DAY. UNFORTUNATELY THE OPERATION WAS NOT COMPLETED. MANUFACTURED DATE: 08 MARCH 2018. LOT SIZE: (B)(4) UNITS. PURCHASE DATE: (B)(6) 2018.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7550175 ↗

Other Kit, nephroscope devices

All Kit, nephroscope devices →

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