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Versaport NB3SHFLPRecalls & reported problems

Covidien LP · Bladeless Low Profile Trocar with Fixation Cannula · Class 2

All models of Versaport (21)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 10884521070394), received between Jul 6, 2021 and Jul 6, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

Device problems

  • Detachment of Device or Device Component1
  • Packaging Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJul 6, 2021Detachment of Device or Device Component; Packaging Problem; Detachment of Device or Device Component; Packaging Problem

    ACCORDING TO THE REPORTER, DURING A GENERAL LAPAROSCOPY, ON TROCAR PLACEMENT, THE PLASTIC O RING FROM ONE THE 4 TROCARS FELL INTO THE PATIENT CAVITY AND WAS RETRIEVED BY A LAPAROSCOPIC GRASPER TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12123975 ↗

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Sources and updates

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