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Medline Industries, Inc. DYNJ0166780RRecalls & reported problems

Medline Industries, Inc. · NORTH MINOR 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 10195327021559), received between Mar 24, 2022 and Mar 24, 2022 — classified as 1 injury.

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

  • Break1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryMar 24, 2022Break

    ACCORDING TO THE FACILITY DURING A PROCEDURE AN 18X18 LAP SPONGE 'FELL APART AND HAD TO BE REMOVED FROM THE WOUND DURING SURGERY'. NO ADDITIONAL INFORMATION IS AVAILABLE.

    Patient problems: Foreign Body In Patient

    MAUDE report 13891768 ↗

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Sources and updates

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