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Hickman 0600320Recalls & reported problems

Bard Access Systems, Inc. · Hickman 9 Fr Pediatric Length Dual-Lumen CV Catheter, Cutdown Tray with SureCuff Tissue Ingrowth Cuff · Class 2 · Implant

All models of Hickman (28)

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 00801741051746), received between Feb 13, 2018 and Feb 13, 2018 — classified as 1 malfunction.

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

  • Crack1
  • Loose or Intermittent Connection1
  • Material Rupture1

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.

  • MalfunctionFeb 13, 2018Crack; Loose or Intermittent Connection; Material Rupture

    IT WAS REPORTED THAT THE CATHETER WAS LOOSE AND RUPTURED AND NOTED TO BE CRACKED AT THE Y-SITE. NO PATIENT INJURY REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7267949 ↗

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

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Sources and updates

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