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Medline Industries, Inc. DYNJ65593ARecalls & reported problems

Medline Industries, Inc. · INTERVENTIONAL TRAY · 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 10193489473896), received between Mar 9, 2023 and Mar 9, 2023 — classified as 1 injury.

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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1

Recent adverse event reports

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

  • InjuryMar 9, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ACCORDING TO THE FACILITY ON (B)(6) 2023 DURING AN ANEURYSM EMBOLIZATION "FIBERS CAME LOOSE BUT DID NOT EXIT THE MICRO CATHETER INTO THE PATIENT, THE MICRO CATHETER AND WIRE WERE REMOVED WHEN IT WAS DISCOVERED TO HAVE DIFFICULTIES MOVING THE MICRO WIRE, AND ON THE BACK TABLE THE MICRO CATHETER WAS FLUSHED WITH SALINE AND A SMALL PIECE OF LINT WAS EXPELLED OUT OF THE CATHETER".

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 16516847 ↗

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Sources and updates

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