Memory Basket G22074Recalls & reported problems
Cook Incorporated · Memory Hard Wire Basket · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00827002220744), received between Apr 30, 2025 and May 13, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fracture” (2 reports).
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
Most reported problems
Device problems
- Fracture2
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 13, 2025Break; Break
DURING AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP) IN THE COMMON BILE DUCT, THE PHYSICIAN USED A COOK MEMORY HARD WIRE BASKET. IT WAS INITIALLY REPORTED THAT DURING THE PROCEDURE THE USER DETECTED THE BASKET COULD NOT BE OPENED COMPLETELY AND COULD NOT REMOVE THE STONE. THE USER CHANGED TO ANOTHER SAME RPN DEVICE TO CONTINUE THE STONE REMOVAL. THERE WAS NO REPORTABLE INFORMATION AT THAT TIME. THE DEVICE WAS RECEIVED FOR EVALUATION ON 21 APR 2025 WITH THE BASKET PARTIALLY EXTENDED AND THE BASKET COULD NOT BE RETRACTED USING THE HANDLE [SUBJECT OF REPORT]. A SECTION OF THE DEVICE DID NOT REMAIN INSIDE THE PATIENT¿S BODY. THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22013494 ↗MalfunctionApr 30, 2025Fracture; Fracture
DURING AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP)FOR STONE REMOVAL IN THE COMMON BILE DUCT, THE PHYSICIAN USED A COOK MEMORY HARD WIRE BASKET. IT WAS REPORTED THAT AT BEGINNING OF STONE REMOVAL USER DETECTED THE ONE BASKET WIRE BROKEN. THE USER CHANGED TO ANOTHER BASKET TO CONTINUE THE PROCEDURE. A SECTION OF THE DEVICE DID NOT REMAIN INSIDE THE PATIENT¿S BODY. THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21937077 ↗MalfunctionApr 30, 2025Fracture; Fracture
DURING AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP)FOR STONE REMOVAL IN THE COMMON BILE DUCT, THE PHYSICIAN USED A COOK MEMORY HARD WIRE BASKET. IT WAS REPORTED THAT AT BEGINNING OF STONE REMOVAL USER DETECTED THE ONE BASKET WIRE BROKEN. THE USER CHANGED TO ANOTHER BASKET TO CONTINUE THE PROCEDURE. A SECTION OF THE DEVICE DID NOT REMAIN INSIDE THE PATIENT¿S BODY. THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21937031 ↗
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- NGage G48294Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL92 reports
- NCircle G19110Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL88 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.