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Pro-PICC® CT MR17036306MBRecalls & reported problems

Medical Components, Inc. · 6F X 60CM TRIPLE PRO-PICC® CT FULL NURSING TRAY W/MAX BARRIER · Class 2 · Implant

All models of Pro-PICC CT (12)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884908083378), received between Jun 13, 2017 and Sep 20, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1
  • Hole In Material1
  • Leak/Splash1

Patient problems

  • No Information1
  • No Known Impact Or Consequence To Patient1
  • Swelling1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 20, 2018Fracture; Fracture

    THERE IS A RUPTURE IN THE LINE APPROXIMATELY 2CM FROM THE HUB.

    Patient problems: Swelling

    MAUDE report 7893132 ↗
  • MalfunctionJun 13, 2017Hole In Material; Leak/Splash

    WHEN FLUSHING PICC IMMEDIATELY AFTER PLACEMENT NOTICED LEAKING AND HOLE AT SITE WHERE PICC JOINS HUB.

    Patient problems: No Information; No Known Impact Or Consequence To Patient

    MAUDE report 6636378 ↗

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

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