PANOVIEW 8970407Recalls & reported problems
Richard Wolf GmbH · MORCESCOPE 0° 24FR WL 199MM rigid, with parallel ocular lens, working channel for instruments up to 4.8mm, irrigation via 24.5/26Ch sheath and attachement, suction via morcellator, TL 393mm, rod lens system · Class 2
All models of PANOVIEW (10)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04055207055113), received between Aug 27, 2024 and Aug 27, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Poor Quality Image” (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.
Reports received per month
Most reported problems
Device problems
- Poor Quality Image1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 27, 2024Poor Quality Image; Poor Quality Image
RICHARD WOLF GMBH (RWGMBH) HAS RECEIVED A "USER-NOTIFICATION" REPORT NO. (B)(4) FROM AN IMPORTER, AMT SURGICAL IN CANADA. THE REPORTED ISSUE IS REGARDING A MORCESCOPE 0° 24FR WL 199MM, PART ID: 8970407, SN# (B)(6). ACCORDING TO THE RECEIVED INFORMATION, THE MORCELATOR SCOPE WAS BLURRY, AND THE SURGEON COULD NOT VISUALIZE FIELD IN ORDER TO CONTINUE PROCEDURE. ALSO, COULD NOT TURN OVER OTHER SCOPE IN AN APPROPRIATE PERIOD. LATER, RWGMBH RECEIVED INFORMATION THAT THE PATIENT'S SURGICAL PROCEDURE WAS CANCELLED WHILE NOT COMPLETED, AND HAD TO BE RESCHEDULED TO COMPLETE THE OPERATION.
Patient problems: Insufficient Information
MAUDE report 20080270 ↗
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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page