Skip to content

Medline Industries, Inc. DYNJ900356QRecalls & reported problems

Medline Industries, Inc. · EAR CDS · 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 10195327098001), received between Sep 28, 2022 and Sep 28, 2022 — 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

  • 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.

  • InjurySep 28, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ACCORDING TO THE FACILITY DURING THE MIDDLE OF A PROCEDURE, 'THE BLADE BROKE OFF IN THE MIDDLE EAR AND WAS RETRIEVED WITH AN INSTRUMENT'.

    Patient problems: Foreign Body In Patient

    MAUDE report 15498375 ↗

Other Ear, nose, and throat surgical tray devices

All Ear, nose, and throat surgical tray devices →

Sources and updates

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