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PowerPICC Provena CK000765Recalls & reported problems

Bard Access Systems, Inc. · Catheter Placement Kit · Class 2 · Implant

All models of PowerPICC Provena (116)

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 00801741141744), received between Dec 22, 2017 and Dec 22, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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

  • Fluid/Blood Leak1

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 22, 2017Fluid/Blood Leak

    IT WAS REPORTED THAT THE PATIENT WAS RECEIVING CONTINUOUS INFUSION OF TPN FOR SEVERAL WEEKS, WHEN THE VALVE BEGAN LEAKING. TPN WAS GETTING ON THE PATIENT'S DRESSING. THE VALVE WAS REPLACED AND THEY NOTED THAT A BUBBLE OF FLUID APPEARED ON THE LUMEN; WHERE THE LUMEN CONNECTS TO THE TUBING. WITH CONTINUED FLUSHING, NEW FLUID BUBBLES APPEARED. THERE WAS NO LEAKING FROM THE VALVE. TPN WAS STOPPED AND THE PICC WAS REPLACED. NO PATIENT INJURY REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7143911 ↗

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Sources and updates

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