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Medline Industries, Inc. DYNJ0428947FRecalls & reported problems

Medline Industries, Inc. · BREAST ABDOMINOPLASTY MZ PK-LF · Class 1

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 10889942541584), received between Aug 15, 2018 and Aug 15, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

  • Device Contamination with Chemical or Other Material1

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.

  • MalfunctionAug 15, 2018Device Contamination with Chemical or Other Material

    IT WAS REPORTED THAT PRIOR TO THE CLOSING OF THE SURGICAL SITE, IRRIGATION WAS REQUIRED TO SUCCESSFULLY REMOVE LINT COMING FROM THE LAP SPONGES.

    Patient problems: Foreign Body In Patient

    MAUDE report 7784939 ↗

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Sources and updates

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