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Memory G57268Recalls & reported problems

Cook Incorporated · Memory Hard Wire Basket · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002572683), received between Aug 25, 2022 and Aug 25, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Remove” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Difficult to Remove1

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.

  • InjuryAug 25, 2022Difficult to Remove; Adverse Event Without Identified Device or Use Problem; Difficult to Remove; Adverse Event Without Identified Device or Use Problem

    DURING AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP), THE PHYSICIAN USED A COOK MEMORY HARD WIRE BASKET. IT WAS REPORTED THAT THE BASKET WITH STONE BECAME STUCK & WOULD NOT TRAVERSE THE AMPULLA. ACCORDING TO THE INITIAL REPORTER, THE PHYSICIAN CUT HANDLE OFF, REMOVED THE SCOPE, TRANSFERRED THE PATIENT TO A FACILITY WITH ADVANCED LITHOTRIPSY AND THE PATIENT WAS REPORTED TO NOT HAVE EXPERIENCED ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.

    Patient problems: Foreign Body In Patient

    MAUDE report 15294757 ↗

Other DISLODGER, STONE, BILIARY devices

All DISLODGER, STONE, BILIARY devices →

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