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Medline Industries, Inc. DYNJ901310DRecalls & reported problems

Medline Industries, Inc. · MINOR · 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 10889942565238), received between Aug 24, 2023 and Aug 24, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Thermal Decomposition of Device” (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

  • Thermal Decomposition of Device1

Patient problems

  • Superficial (First Degree) Burn1

Recent adverse event reports

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

  • InjuryAug 24, 2023Thermal Decomposition of Device; Thermal Decomposition of Device

    ACCORDING TO THE CUSTOMER, WHILE USING THE CAUTERY DEVICE ON 07/31/2023 "TWO HOLES BURNED THROUGH THE SHAFT OF THE CAUTERY TIP CAUSING THREE SMALL (0.5 CM) SUPERFICIAL BURN MARKS ON THE PATIENT'S NIPPLE AND AREOLA".

    Patient problems: Superficial (First Degree) Burn

    MAUDE report 17618467 ↗

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Sources and updates

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