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VersaSeal Plus 175772PRecalls & reported problems

Covidien LP · Cannula Seal · 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 20884521082592), received between May 30, 2018 and May 30, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment Of 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment Of Device Component1

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.

  • MalfunctionMay 30, 2018Detachment Of Device Component; Detachment Of Device Component

    ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC CHOLECYSTECTOMY, A SMALL PIECE OF BLUE RUBBER SEAL RIPPED OFF FROM INSIDE THE PORT AND GONE IN TO THE PATIENT¿S ABDOMINAL CAVITY AND WAS RETRIEVED USING LAPAROSCOPIC GRASPERS TO COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7553163 ↗

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