n.a. 30114G2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551254769), received between Nov 21, 2019 and Nov 21, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Arcing” (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 21, 2019Arcing; Arcing

  ALLEGEDLY, PER THE CUSTOMER, DURING A LAPAROSCOPIC VENTRAL HERNIA REPAIR, THE TIP OF THE METAL CANNULA WAS BENT WHICH SHAVED OFF INSULATION FROM THE LAP SCISSOR. THE SURGEON HAD TO EXCISE BURNED SKIN LEAVING A SLIGHTLY LARGER SCAR, NO FRAGMENTS WERE LEFT IN THE PATIENT AND A POST OP FOLLOW UP INDICATED THE BURN WAS HEALING WITH NO OTHER INTERVENTION REQUIRED.

  Patient problems: Burn, Thermal

  MAUDE report 9356670 ↗