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MEDLINE DYND44108Recalls & reported problems

Medline Industries, Inc. · TRAP,MUCUS,8FR,DELEE,W/VALVE · Class 2

Data updated Oct 16, 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 10080196997411), received between Jan 21, 2020 and Jan 20, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Connection Problem” (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

  • Connection Problem1
  • Entrapment of Device1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Foreign Body Sensation in Eye1

Recent adverse event reports

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

  • InjuryJan 20, 2023Connection Problem; Connection Problem

    ACCORDING TO THE FACILITY THERE WAS A DELAY IN SUCTIONING A NEWBORN DUE TO THE "DEVICE NOT STAYING CONNECTED TO THE SUCTION TUBING."

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

    MAUDE report 16218595 ↗
  • InjuryJan 21, 2020Entrapment of Device

    IT WAS REPORTED TO THE MANUFACTURER VIA A MEDWATCH FILED BY THE END-USER THAT AN INFANT WAS CHOKING ON A DELEE MUCUS TRAP DEVICE.

    Patient problems: Foreign Body Sensation in Eye

    MAUDE report 9612839 ↗

Other TRAP, STERILE SPECIMEN devices

All TRAP, STERILE SPECIMEN devices →

Sources and updates

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