PRINCESS 8653131Recalls & reported problems
Richard Wolf GmbH · CUTTING ELECTRODE MONO 21FR for hysteroscopy, for continuous irrigation sheaths, 21, Fr, loop: round, wire Ø 0.3mm, fork color red, stem color blue, PACK=1 PC, for use in combination with the Princess resectoscope, unsterile, reusable · 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 04055207042885), received between Feb 10, 2017 and Feb 10, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Handling 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device Handling Problem1
- Material Deformation1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 10, 2017Material Deformation; Device Handling Problem; Material Deformation; Device Handling Problem
Other RESECTOSCOPE, WORKING ELEMENT devices
- S-LINE 8680224Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT7 reports
- E-LINE 86553841Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT7 reports
- S-LINE 8680225Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT5 reports
- S-LINE 8680204Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT5 reports
- S-LINE 8680205Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT1 death5 reports
- NA 8654282Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT3 reports
- PRINCESS 8653018Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT2 reports
- SHARK 8674225Richard Wolf GmbH · RESECTOSCOPE, WORKING ELEMENT2 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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