Cold Snare CS3-21023230Recalls & reported problems

Micro-Tech (Nanjing) Co., Ltd. · Oval,Diameter of Snare is 10 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 06932503550031), received between Dec 29, 2025 and Dec 29, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (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.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Material Twisted/Bent1

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.

MalfunctionDec 29, 2025Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT MICRO TECH COLD SNARE OPENED IN PATIENT- NOTICED THE TIP OF SNARE WAS BENT AND FOLDED OVER ONTO ITSELF. DEFECTIVE DEVICE, SNARE WAS REMOVED FROM PATIENT, WASTED AND REPLACED WITH A PROPER WORKING SUPPLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23904635 ↗

Device details

UDI-DI	`06932503550031`
Brand	Cold Snare
Model	CS3-21023230
Company	Micro-Tech (Nanjing) Co., Ltd.
Product code	GAE · Snare, Surgical
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Dec 3, 2025

Device type (GMDN): Mechanical-cutting endoscopic polypectomy snare

A sterile, flexible, non-powered (i.e., not electrosurgical) device intended to be inserted through an endoscope to ensnare and cut polyps or other mucosal lesions during endoscopic surgery. It typically consists of a flexible sheath with a sharp cutting snare loop attached to the distal end of the sheath, and a handle which mechanically controls snaring through manual action. This is a single-use device.

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All Snare, Surgical devices →

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