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Medline Industries, Inc. DYNJ44804FRecalls & reported problems

Medline Industries, Inc. · GEN CV LAPAROSCOPY 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 10195327323325), received between Apr 6, 2023 and Apr 6, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination” (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

  • Contamination1

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.

  • MalfunctionApr 6, 2023Contamination

    A FOREIGN BODY WAS FOUND ON THE TOWEL IN THE PACK. NEITHER THE PACK NOR THE FOREIGN BODY WAS SAVED. DID NOT PRESENT ANY ADVERSE OUTCOMES FOR THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16688909 ↗

Other laparoscopy kit devices

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Sources and updates

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