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Medline Industries, Inc. DYNJ60102CRecalls & reported problems

Medline Industries, Inc. · ARTHRO PACK · Class 1

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 10195327356170), received between Jul 26, 2023 and Jul 26, 2023 — 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.

  • InjuryJul 26, 2023Break; Break

    ACCORDING TO THE CUSTOMER, WHEN USING AN "11 BLADE" FROM THE ARTHROSCOPY PACK, IT "BROKE IN HALF."

    Patient problems: Foreign Body In Patient

    MAUDE report 17401367 ↗

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Sources and updates

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