Versaport 177092FRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884521094403), received between Jun 11, 2019 and Jun 11, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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.

• MalfunctionJun 11, 2019Difficult to Insert; Difficult to Insert

  ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC CHOLECYSTECTOMY, WHEN THE SURGEON TRIED TO REMOVE THE SUCTION/IRRIGATION SYSTEM FROM THE 5MM-TROCAR HE WAS NOT ABLE NOT PULL THE INSTRUMENT OUT OF THE TROCAR. HE HAD TO REMOVE THE WHOLE TROCAR WITH THE INSTRUMENT. THERE WAS NO PATIENT INJURY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8688004 ↗