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PowerPICC CK000130Recalls & reported problems

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

All models of PowerPICC (118)

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 00801741042607), received between Jul 19, 2017 and Jul 19, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Damaged Prior to Use” (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

  • Device Damaged Prior to Use1
  • Out-Of-Box Failure1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionJul 19, 2017Device Damaged Prior to Use; Out-Of-Box Failure

    FACILITY REPORTED TO THE SALES REP THAT THE PICC WAS REMOVED FROM THE PACKAGE AND THE HEALTHCARE PROFESSIONAL NOTED THAT THE PICC HAD A VISIBLE BUBBLE FROM THE PRELOADED STYLET. DEVICE WAS NOT USED ON THE PATIENT AND WAS SET ON THE SIDE TABLE. WHEN SETTING THE DEVICE ON THE TABLE IT "BROKE".

    Patient problems: No Patient Involvement

    MAUDE report 6726334 ↗

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Sources and updates

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