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Cook G14335Recalls & reported problems

Cook Incorporated · Coaxial Sheath Grasping Forceps · Class 2

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 00827002143357), received between Sep 25, 2018 and Sep 25, 2018 — classified as 1 malfunction.

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

  • Collapse1

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.

  • MalfunctionSep 25, 2018Collapse; Collapse

    IT WAS REPORTED, DURING A URETEROSCOPY, THE WIRES AT THE END OF THE NCIRCLE TIPLESS STONE EXTRACTOR BASKET WERE COLLAPSING ON THEMSELVES WHILE IN THE OPEN POSITION. THEY WOULD NOT HOLD THEIR SHAPE. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH ANOTHER DEVICE OF THE SAME TYPE. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE ALLEGED MALFUNCTION.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7906002 ↗

Other DISLODGER, STONE, BASKET, URETERAL, METAL devices

All DISLODGER, STONE, BASKET, URETERAL, METAL devices →

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