Olympus WA22723SRecalls & reported problems
OLYMPUS Winter & Ibe GmbH · HF-resection electrode PlasmaBand band, medium, 24 Fr., 12°-30°, ESG TURis · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 14042761085387), received between Apr 17, 2025 and Apr 22, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (3 reports).
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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 22, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING A TRANSURETHERAL RESECTION OF PROSTRATE THERAPEUTIC PROCEDURE, THE LOOPS OF THE ELECTRODE OF THE HIGH-FREQUENCY ELECTRODE (PLASMABAND) FELL OFF. THE PROCEDURE WAS COMPLETED WITH A REPLACEMENT DEVICE. THERE WAS NO REPORT OF PATIENT HARM OR USER INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21884733 ↗MalfunctionApr 21, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THE LOOPS OF THE HF(HIGH FREQUENCY)-RESECTION ELECTRODE WERE FALLING OFF. THE ISSUE OCCURRED DURING A THERAPEUTIC TRANSURETHRAL RESECTION OF PROSTATE PROCEDURE. THE PROCEDURE WAS COMPLETED USING A SIMILAR DEVICE. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21871071 ↗MalfunctionApr 17, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE RESECTION ELECTRODE LOOPS FELL OFF. THIS ISSUE OCCURRED DURING A THERAPEUTIC TRANSURETHRAL RESECTION OF PROSTRATE PROCEDURE. THERE WAS A DELAY OF LESS THAN 30 MINUTES, AND THE PROCEDURE WAS COMPLETED WITH A SIMILAR DEVICE. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21856568 ↗
Other Electrode, Electrosurgical, Active, Urological devices
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- Olympus WA22603SOLYMPUS Winter & Ibe GmbH · Electrode, Electrosurgical, Active, Urological1 recall7 reports
- Olympus WA22621SOLYMPUS Winter & Ibe GmbH · Electrode, Electrosurgical, Active, Urological1 recall4 reports
- Olympus WA22305SOLYMPUS Winter & Ibe GmbH · Electrode, Electrosurgical, Active, Urological1 recall3 reports
- Olympus WA22657SOLYMPUS Winter & Ibe GmbH · Electrode, Electrosurgical, Active, Urological1 recall2 reports
- Olympus WA22332DOLYMPUS Winter & Ibe GmbH · Electrode, Electrosurgical, Active, Urological1 recall2 reports
- Olympus WA22301DOLYMPUS Winter & Ibe GmbH · Electrode, Electrosurgical, Active, Urological1 recall2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.