Captura Pro G47696Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827002476967), received between Feb 7, 2025 and Mar 27, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Open or Close” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 27, 2025Difficult to Open or Close; Component Misassembled; Difficult to Open or Close; Component Misassembled

  DURING AN ENDOSCOPIC PROCEDURE TO TAKE BIOPSY SAMPLES IN THE DUODENUM, THE PHYSICIAN USED A COOK CAPTURA PRO BIOPSY FORCEPS WITH SPIKE. IT WAS REPORTED THAT WHEN THEY WANT TO CLOSE, IT TOOK TIME AND THEY FELT LOT OF RESISTANCE. IT WAS STUCK OPEN. 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 21704558 ↗
• MalfunctionFeb 7, 2025Difficult to Open or Close; Difficult to Open or Close

  DURING AN ENDOSCOPIC PROCEDURE TO TAKE BIOPSY SAMPLES IN THE DUODENUM, THE PHYSICIAN USED 2 COOK CAPTURA PRO¿ BIOPSY FORCEPS WITH SPIKE. IT WAS REPORTED THAT ONCE THE FIRST DEVICE HAD PASSED THE CANAL OF THE ENDOSCOPE, IT COULD BE OPENED BUT THEN IT COULD NOT CLOSE. THE SECOND DEVICE COULD OPEN WELL, BUT WHEN THEY WANTED TO CLOSE, IT TOOK TIME AND THEY FELT A LOT OF RESISTANCE. BOTH PRODUCTS WERE USED IN THE SAME 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 21335323 ↗