Skip to content

PRINCESS 46531323Recalls & reported problems

Richard Wolf GmbH · CUTTING ELECTRODE BIPO 24.5FR for hysteroscopy, for continuous irrigation sheaths, 24.5, Fr, loop: round, wire Ø 0.3mm, fork color transparent, stem color blue, PACK=3 PCS, for use in combination with the Princess resectoscope, sterile, for single use · 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 04055207048979), received between Jun 21, 2021 and Jun 21, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping 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

  • Appropriate Device Problem Term/Code Not Available1
  • Manufacturing, Packaging or Shipping 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.

  • MalfunctionJun 21, 2021Manufacturing, Packaging or Shipping Problem; Appropriate Device Problem Term/Code Not Available; Manufacturing, Packaging or Shipping Problem; Appropriate Device Problem Term/Code Not Available

    THE PURPOSE OF THIS REPORT IS TO SHARE THE RESULTS OF THE PRODUCT HISTORY REPORT FROM RW GMBH. SEE MANUFACTURERS NARRATIVE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12035643 ↗

Other ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL devices

All ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL devices →

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