Skip to content

BARD Poly Midline 4154108Recalls & reported problems

Bard Access Systems, Inc. · Bard Poly Midline 4F Single-Lumen Full Kit (20 cm) · Class 2

All models of Bard Poly Midline (9)

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 00801741037658), received between Jan 27, 2021 and Jan 27, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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

  • Material Split, Cut or Torn1

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.

  • MalfunctionJan 27, 2021Material Split, Cut or Torn

    IT WAS REPORTED "THE GLOVES IN THE KIT KEEP RIPPING" ADDITIONAL INFO. RECEIVED 01/04/2021: "THERE WAS NO HARM TO PATIENT, NEW GLOVES WERE OBTAINED AND PROCEDURE COMPLETED. THE GLOVES RIPPED AND WERE THROWN AWAY. THE OCCURRENCE HAPPENED MOST OF DECEMBER WITH REEW2786 LOT NUMBERS ON MIDLINE KITS."

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 11236630 ↗

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