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PowerPICC SOLO CK000291BRecalls & reported problems

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

All models of PowerPICC SOLO (78)

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 00801741132087), received between Apr 13, 2017 and Apr 13, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Break1
  • Difficult To Position1

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.

  • MalfunctionApr 13, 2017Break; Difficult To Position

    FACILITY REPORTED TO THE SALES REP THAT THE NURSE WAS EXPERIENCING DIFFICULTY PLACING A PICC IN THE PATIENT. THE NURSE REMOVED THE GUIDEWIRE AND WAS CLEANING THE BLOOD CLOT OFF OF THE END OF THE WIRE AND THE WIRE BROKE OFF IN HER HAND. NO PATIENT INJURY WAS REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6489882 ↗

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Sources and updates

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