Olympus A3764ARecalls & reported problems
OLYMPUS Winter & Ibe GmbH · Telescope, 1.9 mm, 0°,210mm, autoclavable · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04042761005722), received between Mar 30, 2023 and Nov 20, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (2 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
- Break2
- Crack1
- Sharp Edges1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 20, 2025Sharp Edges; Sharp Edges
IT WAS OBSERVED THAT DURING THE DEVICE EVALUATION, THE TELESCOPE EXHIBITED SHARP EDGES ON THE DISTAL END. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23610233 ↗MalfunctionJul 9, 2025Break; Break
IT WAS REPORTED THAT DURING INSPECTION FOR USE THE SUBJECT DEVICE HAD BROKEN FIBERS. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22460748 ↗MalfunctionNov 20, 2023Break; Break
THE CUSTOMER REPORTED TO OLYMPUS, THE TELESCOPE, 1.9 MM, 0°,210MM, WAS SMASHED AT THE FRONT OF THE OPTIC. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18167495 ↗MalfunctionMar 30, 2023Crack; Crack
THE CUSTOMER REPORTED THE AUTOCLAVABLE TELESCOPE WAS FOUND TO HAVE A ¿LENS CRACK¿ DURING INSPECTION BEFORE USE. THE SCOPE WAS REPLACED, AND THE INTENDED STENT REMOVAL PROCEDURE WAS COMPLETED. A FIVE-MINUTE DELAY WAS REPORTED WITH NO DEATH OR INJURY AND NO IMPACT TO PATIENT OR OTHER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16651270 ↗
Other Resectoscope devices
- Olympus A22040AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall1,764 reports
- Olympus A42011AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall963 reports
- Olympus A22041AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall656 reports
- Olympus A22042AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall55 reports
- Olmypus WA22017AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall31 reports
- Olympus A22040TOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall23 reports
- Olympus A22041TOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall12 reports
- Olympus A22014AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall11 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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