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Bluntport Plus 176626PRecalls & reported problems

Covidien LP · Blunt Trocar · Class 1

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 20884521081137), received between Dec 4, 2017 and Dec 4, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • No Known Impact Or Consequence 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 4, 2017Break; Break

    ACCORDING TO THE REPORTER, DURING A RIGHT VIDEO-ASSISTED THORACOSCOPIC PROCEDURE, THE TIP OF THE CANNULA BROKE DURING INSERTION. THEY GOT A NEW TROCAR TO COMPLETE THE CASE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7080446 ↗

Other GOUGE, SURGICAL, 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.