Hydro-Surg 5600180Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741077210), received between May 14, 2021 and May 14, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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 18, 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.

• MalfunctionMay 14, 2021Break; Break

  AS REPORTED VIA FDA 3500A FORM REPORT ((B)(4)): " DURING LAPAROSCOPIC CHOLECYSTECTOMY, SURGEON USING SPATULA TIP CAUTERY TO REMOVE GALLBLADDER. TIP BROKE OFF THE SPATULA. TIP RETRIEVED IMMEDIATELY WITH NO HARM TO PATIENT. " ADDENDUM PER ADDITIONAL INFORMATION: AS REPORTED, THE BARD/DAVOL CORBITT SPATULA DISTAL ELECTRODE TIP HAD BEEN LOCKED SECURELY INTO PLACE AND WAS USED FOR APPROX. 20 MINUTES PRIOR TO "BREAKING OFF." ANOTHER TIP WAS USED TO COMPLETE THE CASE. NO ALLEGED PATIENT INJURY WAS REPORTED AS A RESULT OF THE PROBLEM EXPERIENCED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11826380 ↗