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Medline Industries, Inc. DYNJ0378596FRecalls & reported problems

Medline Industries, Inc. · CATH LAB DRAPE PACK-LF · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942063024), received between Sep 18, 2018 and Sep 18, 2018 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

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.

  • InjurySep 18, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT DURING A RIGHT AND LEFT HEART CATH PROCEDURE THE FORCEPS PUNCTURED AN UNIDENTIFIED FEMORAL ARTERY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7887313 ↗

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Sources and updates

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