Versaport Plus 179095PFRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884521081298), received between Jun 19, 2017 and Jan 12, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Packaging Problem” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionJan 12, 2021Detachment of Device or Device Component; Packaging Problem; Detachment of Device or Device Component; Packaging Problem

  ACCORDING TO THE REPORTER, PRIOR TO THE PROCEDURE, AFTER REMOVING THE PACKAGING, THE HEAD OF THE OBTURATOR IS SEPARATED WHEN TRYING TO COMBINE THE OBTURATOR AND CANNULA. NEW PRODUCT WAS USED TO RESOLVE THE ISSUE. NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11155777 ↗
• MalfunctionJun 19, 2017Packaging Problem; Packaging Problem

  ACCORDING TO THE REPORTER, DURING A GASTRECTOMY PROCEDURE THE STABBER OF THE TROCAR WAS BROKEN AND THE KNIFE WAS APPEARED. THE PROBLEM NOTICED PRIOR TO USE. THERE WAS NO PATIENT INVOLVEMENT

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6650181 ↗