The Web G22303Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00827002223035), received between Jul 26, 2019 and May 19, 2026 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Material Rupture” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 19, 2026Material Rupture

  DURING AN ENDOSCOPIC PROCEDURE, THE PHYSICIAN USED A COOK WEB II MEMORY EXTRACTION BASKET. IT WAS REPORTED THAT THE PHYSICIAN WAS UNABLE TO FULLY DEPLOY THE BASKET AFTER ADVANCING THE DEVICE INTO THE PATIENT¿S BILE DUCT. WHEN SLIGHT FORCE WAS APPLIED TO EXTEND THE BASKET, IT WAS SUBSEQUENTLY OBSERVED DURING RETRACTION THAT THE INNER CORE HAD PROTRUDED THROUGH THE SHEATH. 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 25216611 ↗
• MalfunctionAug 27, 2025Material Rupture; Material Rupture

  DURING AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY, ERCP, THE PHYSICIAN USED A COOK WEB II MEMORY EXTRACTION BASKET. IT WAS REPORTED THAT DURING AN ATTEMPT TO EXTRACT STONES, THE BASKET WAS MANEUVERING AROUND THE STONE AND ATTEMPTING TO CRUSH IT WHEN THE DRIVE WIRE DETACHED FROM THE HANDLE AND EXITED THE PLASTIC SHEATH. THE DEVICE WAS REMOVED, THE PROCEDURE WAS HALTED, AND IT COULD NOT BE COMPLETED. 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 22903154 ↗
• MalfunctionSep 18, 2019Material Split, Cut or Torn; Material Split, Cut or Torn

  DURING AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP), THE PHYSICIAN USED A COOK WEB II MEMORY EXTRACTION BASKET. THE TECHNICIAN FOUND THE BASKET'S HANDLE WAS STUCK AND COULD NOT OPEN THE BASKET. HE WITHDREW IT AND USED A NEW ONE. THERE WAS NO REPORTABLE INFORMATION AT THIS TIME. THE DEVICE WAS EVALUATED ON (B)(6) 2019. THE DRIVE WIRE HAD RUPTURED THROUGH THE CATHETER ON THE PROXIMAL END OF THE DEVICE. 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 Consequences Or Impact To Patient

  MAUDE report 9083460 ↗
• InjuryJul 26, 2019Material Split, Cut or Torn; Material Split, Cut or Torn

  DURING A STONE RETRIEVAL PROCEDURE, THE PHYSICIAN USED A COOK WEB II MEMORY EXTRACTION BASKET. ONCE THE STONE WAS RETRIEVED, AND THE NURSE STARTED TO CLOSE THE BASKET, THE PLASTIC SHEATH BROKE NEAR THE HANDLE, THUS IT WAS NOT POSSIBLE TO EXTRACT THE BASKET NOR THE STONE. PART OF THE WIRES OF THE BASKET CAME OUT AND IT WAS NOT POSSIBLE TO RE-OPEN THE BASKET. THEY CUT THE HANDLE TO REMOVE THE ENDOSCOPE. THE PATIENT HAD TO UNDERGO SURGERY TO REMOVE IT [THE BASKET AND BILIARY STONE]. THE EXTRACTION BASKET REMAINED INSIDE THE PATIENT¿S BODY. THE PATIENT REQUIRED SURGERY TO REMOVE THE BASKET AND BILIARY STONE DUE TO THIS OCCURRENCE. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.

  Patient problems: Foreign Body In Patient

  MAUDE report 8833404 ↗