Skip to content

Cold Snare CS3-11523230Recalls & reported problems

Micro-Tech (Nanjing) Co., Ltd. · Rhombus,Diameter of Snare is 15 mm,Outer tube is PE, diameter is 7Fr,working length is 2300mm,Non-Rotation Type · Class 1

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 06932503550024), received between Jun 23, 2022 and Jun 23, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanics Altered” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Mechanics Altered1
  • Unexpected Therapeutic Results1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 23, 2022Unexpected Therapeutic Results; Mechanics Altered

    IT WAS REPORTED THAT SNARE GOT STUCK ON POLYP, THEY HAD TO CUT THE END OF THE SNARE AND SENT HIM TO SURGERY.

    Patient problems: Foreign Body In Patient

    MAUDE report 14785665 ↗

Other Snare, Surgical devices

All Snare, Surgical devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.