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Medical Action Industries 75378Recalls & reported problems

Medical Action Industries Inc. · 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 10809160022221), received between Apr 18, 2018 and Apr 18, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

  • Device Contamination with Chemical or Other Material1

Patient problems

  • No Known Impact Or Consequence 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 18, 2018Device Contamination with Chemical or Other Material

    WHEN NEW TRACH CARE TRAY WAS OPENED, THERE IS BROWN SUBSTANCE ON THE CONTENTS OF THE PACKAGE. THE CONTENTS APPEAR DIRTY. THIS WAS NOT UTILIZED ON A PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7439477 ↗

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Sources and updates

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