Cook G46203Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002462038), received between Jul 20, 2017 and Jul 20, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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. 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 20, 2017Device Operates Differently Than Expected; Device Dislodged or Dislocated; Device Operates Differently Than Expected; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PHYSICIAN WAS PERFORMING A TRANSURETHRAL RESECTION OF BLADDER TUMOR (TURBT) PROCEDURE BY USING A COOK CUTTING LOOP. THE PHYSICIAN NOTICED THAT THE COOK CUTTING LOOP DISENGAGED FROM THE RESECTOSCOPE, WHICH CAUSED LOSS OF ELECTRIC CURRENT. THE PHYSICIAN USED A DIFFERENT MANUFACTURER¿S CUTTING LOOP TO COMPLETE THE PROCEDURE. NO UNINTENDED SECTION OF THE DEVICE REMAINED INSIDE THE PATIENT'S BODY. THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6727839 ↗