n.a. 37470DLRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551155752), received between May 6, 2020 and May 6, 2020 — classified as 1 malfunction.

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

• MalfunctionMay 6, 2020Material Integrity Problem; Material Integrity Problem

  ALLEGEDLY, PER THE CUSTOMER DURING A LAPAROSCOPIC PROCEDURE WHILE USING THE CANNULA AND SUCTION & COAGULATION HOOK AN AREA NOT INTENDED TO BE CAUTERIZED WAS IN FACT CAUTERIZED. THE SITE WAS OBSERVED, THE PROCEDURE COMPLETED WITH NO HARM TO PATIENT AND NO FURTHER INTERVENTION REQUIRED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10029323 ↗