Skip to content

PowerPICC SOLO CK000045ARecalls & 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 00801741087134), received between Nov 25, 2020 and Nov 25, 2020 — 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 16, 2026.

Most reported problems

Device problems

  • Fluid/Blood Leak1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • 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.

  • MalfunctionNov 25, 2020Fluid/Blood Leak

    IT WAS REPORTED CUSTOMER REPORTS INTRAVENOUS FLUID LEAKED FROM HOLE IN EXTENSION LEG ON RED PORT OF DUAL LUMEN SOLO POWER PICC. LEAK WAS NOTICED UPON FLUSHING LUMEN TO CONFIRM PATENCY DURING INSERTION PROCEDURE. PICC WAS IMMEDIATELY REMOVED AND RETAINED BY CUSTOMER AND A NEW PICC WAS INSERTED USING GUIDEWIRE EXCHANGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

    MAUDE report 10907310 ↗

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