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Medline Industries, Inc. DYNJ43141ARecalls & reported problems

Medline Industries, Inc. · TONSILLECTOMY TRAY · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277233713), received between May 10, 2018 and May 10, 2018 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Insufficient Device Problem Information1

Patient problems

  • Burn(s)2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 10, 2018Insufficient Device Problem Information

    IT WAS REPORTED THAT THE PATIENT EXPERIENCED A SMALL BURN TO THE TONGUE DURING A TONSILLECTOMY PROCEDURE.

    Patient problems: Burn(s)

    MAUDE report 7502955 ↗
  • InjuryMay 10, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT EXPERIENCED A SMALL BURN TO THE TONGUE DURING A TONSILLECTOMY PROCEDURE.

    Patient problems: Burn(s)

    MAUDE report 7502537 ↗

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Sources and updates

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