Uvision Hysteroscope Cable 20050Recalls & reported problems
Uvision 360, Inc. · 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 00853277008022), received between Mar 21, 2023 and Mar 21, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Erratic or Intermittent Display” (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
- Erratic or Intermittent Display1
- No Display/Image1
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.
MalfunctionMar 21, 2023Erratic or Intermittent Display; No Display/Image; Erratic or Intermittent Display; No Display/Image
DR. MACHIN WAS PERFORMING AN IUD REMOVAL AND THE IMAGE ON THE MONITOR WENT OUT. THE STAFF WAS ABLE TO MOVE THE CORD AND THE IMAGE RE-APPEARED TO COMPLETE THE PROCEDURE. THE PATIENT HAS BEEN REPORTED AS DOING FINE. THE PHYSICIAN REPORTED NO INJURY OR IMPACT TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16587903 ↗
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- Olympus A22002AOLYMPUS Winter & Ibe GmbH · Hysteroscope (And Accessories)297 reports
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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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