Skip to content

Medline Industries, Inc. DYNJ901880DRecalls & reported problems

Medline Industries, Inc. · LAG MINOR PROCEDURE · 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 10889942974344), received between Apr 11, 2019 and Apr 11, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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 Separation1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionApr 11, 2019Material Separation

    IT WAS REPORTED THAT THE GAUZE WAS SHREDDING AND THIS REACHED THE SURGICAL SITE. THE SHREDDING WAS SUCCESSFULLY REMOVED FROM THE SURGICAL SITE THROUGH USE OF FORCEPS.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8506042 ↗

Other General surgery tray devices

All General surgery tray devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page