Skip to content

PowerPICC SOLO CK000248Recalls & reported problems

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

All models of PowerPICC SOLO (78)

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 00801741043680), received between Aug 8, 2016 and Aug 8, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Advance” (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

  • Failure to Advance1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionAug 8, 2016Failure to Advance

    FACILITY CONTACT REPORTED TO SALES REPRESENTATIVE THAT DURING A PROCEDURE THE TIP OF WIRE WOULD NOT THREAD THROUGH THE NEEDLE. A NEW WIRE WAS PULLED FROM A NEW KIT. NO PATIENT HARM. SAMPLE EVALUATION REVEALS A FRAYED GUIDEWIRE TIP AND PRESENCE OF BLOOD RESIDUE, INDICATING THIS COMPONENT WAS LIKELY USED ON A PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 5855148 ↗

Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices

All Catheter,intravascular,therapeutic,long-term greater than 30 days devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page