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BARD Poly Midline CK000523Recalls & reported problems

Bard Access Systems, Inc. · Catheter Placement Kit · 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 00801741101304), received between Aug 1, 2017 and Aug 1, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment Of Device Component” (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

  • Detachment Of Device Component1

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.

  • MalfunctionAug 1, 2017Detachment Of Device Component

    PER SALES REP, THE FACILITY REPORTED THAT THE CATHETER CAME APART BELOW THE HUB WHILE INSERTED IN THE PATIENT. THE CATHETER WAS REMOVED WITH NO REPORT OF HARM TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6758900 ↗

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Sources and updates

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