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Acusnare G22897Recalls & reported problems

Cook Incorporated · Acusnare Polypectomy Snare Needle Tip · Class 2

Data updated Oct 13, 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 00827002228979), received between Jun 17, 2016 and Jun 17, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Conduct” (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

  • Failure to Conduct1

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.

  • MalfunctionJun 17, 2016Failure to Conduct; Failure to Conduct

    DURING A ENDOSCOPIC PROCEDURE, THE PHYSICIAN USED A ACUSNARE POLYPECTOMY SNARE NEEDLE TIP. THE EQUIPMENT WAS CONNECTED TO THE ELECTRIC KNIFE [SNARE] FOR CUTTING THE POLYP, BUT THERE WAS NO POWER.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 5732501 ↗

Other Unit, electrosurgical, endoscopic (with or without accessories) devices

All Unit, electrosurgical, endoscopic (with or without accessories) devices →

Sources and updates

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