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Medline Industries, Inc. DYNJ51730BRecalls & reported problems

Medline Industries, Inc. · PATEWOOD MAJOR BREAST · 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 10889942975662), received between May 1, 2023 and May 1, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Material Integrity 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

  • Material Integrity Problem1

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.

  • InjuryMay 1, 2023Material Integrity Problem; Material Integrity Problem

    ACCORDING TO THE FACILITY ON 04/04/23 THE PATIENT WAS UNDERGOING A PROCEDURE WHEN A "FLUFFY BLOB OF BLUE FUZZ ALMOST 1 CM LONG WAS FOUND IN THE INCISION".

    Patient problems: Foreign Body In Patient

    MAUDE report 16844082 ↗

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Sources and updates

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