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Vital-Port G26441Recalls & reported problems

Cook Incorporated · Vital-Port Vascular Access System, Standard M.R.I. 9.5 Fr · Class 2 · Implant

All models of Vital-Port (11)

Data updated Oct 18, 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 00827002264410), received between Mar 5, 2018 and Mar 5, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Disconnection” (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 18, 2026.

Most reported problems

Device problems

  • Disconnection1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • MalfunctionMar 5, 2018Disconnection; Disconnection

    IT WAS REPORTED THAT A VITAL-PORT INFUSION PORT WAS IMPLANTED IN THE PATIENT. A WEEK LATER, IT WAS DISCOVERED THAT THE CATHETER HAD DISCONNECTED FROM THE PORT. THE PATIENT WAS TRANSFERRED TO ANOTHER HOSPITAL THE NEXT DAY AND ADDITIONAL SURGERY WAS PERFORMED TO REMOVE THE DETACHED CATHETER. NO ADDITIONAL CONSEQUENCES TO THE PATIENT WERE REPORTED.

    Patient problems: Failure of Implant

    MAUDE report 7314662 ↗

Other PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR devices

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Sources and updates

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