Logi - Laparoscopic Instrument System 120-7800Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05051986000435), received between Nov 24, 2017 and Nov 24, 2017 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Component Falling” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 24, 2017Component Falling; Device Slipped

  A DISTRIBUTOR REPORTED A COMPLAINT TO SURGICAL INNOVATIONS. DURING A PROCEDURE UNDERTAKEN AT A HOSPITAL IN (B)(6), A RETAINING RIVET JAW MECHANISM BECAME LOOSE CAUSING A PIECE OF THE DEVICE TO FALL INTO THE PATIENT. ATTEMPTS TO RECOVER THE PIECE OF THE DEVICE HAVE BEEN UNSUCCESSFUL.

  Patient problems: No Information

  MAUDE report 7057452 ↗
• MalfunctionNov 24, 2017Detachment Of Device Component; Component Falling; Difficult to Remove

  A DISTRIBUTOR REPORTED A COMPLAINT TO SURGICAL INNOVATIONS. THE COMPLAINT DETAILS STATE, AN INCIDENT OCCURED AT A HOSPITAL IN (B)(6) WITH A LOGIGRASP (120-7800) DEVICE. A SCREW WHICH CONNECTS THE JAWS FELL DOWN IN THE ABDOMINAL CAVITY (OR IT WAS NOT PRESENT IN THE INSTRUMENT) AND THE JAWS DETACHED FROM THE INSERT. THE SCREW COULD NOT BE FOUND.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7057429 ↗