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SPIDER-NET 0230AMRecalls & reported problems

Conmed Corporation · NAKAO SPIDER-NET RETRIEVAL DEVICE, 2.50 X 5.50 X 230.00 CM · 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 20653405054112), received between Jul 11, 2017 and Jul 11, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionJul 11, 2017Break; Break

    THE CUSTOMER REPORTED THAT DURING USE THE NAKAO SPIDER NET BROKE AND THE SAMPLE (POLYP) WAS DISRUPTED DURING SURGERY. THIS PROHIBITED THE ANATOMY-PATHOLOGICAL ASSESSMENT OF THE POLYP. MULTIPLE COLON-SCOPING CONTROLS WERE REQUIRED. DESPITE THE ATTEMPT TO OBTAIN ADDITIONAL PATIENT/EVENT INFORMATION, THERE HAS BEEN NO ADDITIONAL INFORMATION RECEIVED REGARDING THE PATIENT'S DEMOGRAPHIC INFORMATION OR THE REPORTED INCIDENT. THE DEVICE HAS BEEN DISCARDED BY THE USER FACILITY. THIS REPORT IS RAISED ON THE BASIS OF POTENTIAL INJURY WITH RECURRENCE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6703939 ↗

Other SNARE, NON-ELECTRICAL devices

All SNARE, NON-ELECTRICAL devices →

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