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Versaport 179093FRecalls & reported problems

Covidien LP · V2 Bladed Trocar with Fixation Cannula · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884521081250), received between Dec 26, 2019 and Dec 26, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Difficult to Remove1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 26, 2019Difficult to Remove; Difficult to Remove

    ACCORDING TO THE REPORTER, PRE-OPERATIVELY, ON A LAPAROSCOPIC HYSTEROMYOMA, DURING THE PREPARATION PROCESS, AFTER USING THE SUCTION CATHETER TO ENTER AND EXIT THE TWO TROCARS FOR A WHILE, THE DOCTOR FELT THAT THE SUCTION CATHETER WAS STUCK AND UNABLE TO ENTER AND EXIT. THEY OPENED A NEW PRODUCT TO COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9519534 ↗

Other Laparoscope, general & plastic surgery devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.