Cook G46229Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002462298), received between Nov 29, 2017 and Nov 29, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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.

• MalfunctionNov 29, 2017Material Separation; Material Separation

  THE USER FACILITY REPORTED A METAL PIECE AT THE END OF A COOK CUTTING LOOP ELECTRODE BROKE OFF INSIDE THE WORKING ELEMENT OF THE RESECTOSCOPE VIA A USER FACILITY MEDWATCH. THE PHYSICIAN WAS UNABLE TO GET IT OUT OF THE RESECTOSCOPE IN THE OPERATING ROOM. HOWEVER, THE RESECTOSCOPE WAS BROUGHT DOWN TO THE "CENTRAL STERILE" WHERE THE ELECTRODE WAS ABLE TO BE VISUALIZED AND REMOVED. THE REPORTER WAS UNSURE IF THE DEVICE WAS AVAILABLE FOR RETURN. NO ADVERSE EFFECTS TO THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7069761 ↗