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Medline DYND44180Recalls & reported problems

Medline Industries, Inc. · TRAP,MUCUS SPECIMEN, 80CC · Class 2

Data updated Oct 16, 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 10080196818624), received between Jun 21, 2023 and Jun 21, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Leak/Splash” (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 16, 2026.

Most reported problems

Device problems

  • Leak/Splash1

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.

  • InjuryJun 21, 2023Leak/Splash; Leak/Splash

    ACCORDING TO THE FACILITY ON (B)(6) 2023 "A CYTOLOGY SPECIMEN FROM AN ENDOSCOPY LAB LEAKED MAKING THE SPECIMEN UNUSABLE AND THE PATIENT HAD TO BE BROUGHT BACK THE NEXT DAY FOR A REPEAT PROCEDURE".

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

    MAUDE report 17171670 ↗

Other TRAP, STERILE SPECIMEN devices

All TRAP, STERILE SPECIMEN devices →

Sources and updates

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