NA 242058Recalls & reported problems
Medos International Sàrl · HD EP Arthroscope/Sinuscope compatible with Storz style 2.7mm x 70 deg x 75mm · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886705028153), received between Dec 2, 2024 and Dec 2, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (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
- Display or Visual Feedback Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 2, 2024Display or Visual Feedback Problem; Display or Visual Feedback Problem
IT WAS REPORTED THAT DURING TESTING, IT WAS OBSERVED THAT THE HD EPSCP, 2.7, 70, 75, CW_STORZ DEVICE HAD A POOR IMAGE QUALITY. THE EVENT WAS NOT RELATED TO SURGERY. IT WAS REPORTED THAT THE DEVICE WAS NOT INTENDED FOR HUMAN USE; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2024. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20820009 ↗MalfunctionDec 2, 2024Display or Visual Feedback Problem; Display or Visual Feedback Problem
IT WAS REPORTED THAT DURING TESTING, IT WAS OBSERVED THAT THE HD EPSCP,2.7,70,75,CW_STORZ DEVICE HAD A POOR IMAGE QUALITY. THE EVENT WAS NOT RELATED TO SURGERY. IT WAS REPORTED THAT THE DEVICE WAS NOT INTENDED FOR HUMAN USE; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN (B)(6) 2024. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20819675 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.