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Medline Industries, Inc. DYNJ04393GRecalls & reported problems

Medline Industries, Inc. · MAJOR PACK-LF · 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 10193489624298), received between Jul 5, 2022 and Jul 5, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (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

  • Manufacturing, Packaging or Shipping Problem1

Patient problems

  • Insufficient Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 5, 2022Manufacturing, Packaging or Shipping Problem

    AN EXTRA LAP SPONGE WAS FOUND IN THE MAJOR PACK.

    Patient problems: Insufficient Information

    MAUDE report 14914397 ↗

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Sources and updates

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