Skip to content

Medline Industries, Inc. DYNJ45005Recalls & reported problems

Medline Industries, Inc. · CATH LAB PACK · Class 2

Data updated Oct 18, 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 10888277085428), received between Aug 1, 2018 and Aug 1, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Advance” (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 18, 2026.

Most reported problems

Device problems

  • Failure to Advance1

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, 2018Failure to Advance

    IT WAS REPORTED THAT DURING A TRANS-THORACIC PROCEDURE (DIRECT STICK TO THE AORTA), THE GUIDEWIRE GOT CAUGHT IN THE INTRODUCER NEEDLE, A COMPONENT FROM THE CATH LAB PACK.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7739137 ↗

Other Cardiac catheterization kit devices

All Cardiac catheterization kit devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page