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Medline Industries, Inc. DYNJ46542MRecalls & reported problems

Medline Industries, Inc. · LIVER 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 10193489337402), received between Sep 29, 2021 and Sep 29, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or 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 18, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1
  • Material Split, Cut or Torn1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 29, 2021Detachment of Device or Device Component; Material Split, Cut or Torn

    THE YELLOW SUTURE BOOT SPLIT AND FELL OFF OF THE DEVICE INTO THE PATIENT'S ABDOMEN REQUIRING THE SURGEON TO MANUALLY REMOVE THE SUTURE BOOT FROM THE SURGICAL SITE DURING THE PROCEDURE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12548139 ↗

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Sources and updates

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