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Mallinckrodt 18755Recalls & reported problems

Covidien LP · TaperGuard Oral/Nasal Tracheal Tube Murphy Eye · Class 2

All models of Mallinckrodt (73)

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

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

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 50884522007564), received between Mar 12, 2021 and Sep 19, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Defective Component” (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

  • Defective Component1
  • Disconnection1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

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

  • MalfunctionSep 19, 2023Disconnection; Disconnection

    ACCORDING TO THE REPORTER, THE CONNECTOR TUBE WAS LOOSE AND EASILY DETACHES FROM THE ENDOTRACHEAL TUBE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17773573 ↗
  • MalfunctionMar 12, 2021Defective Component; Defective Component

    ACCORDING TO THE REPORTER, PRIOR TO USE, THE DEVICE HAD A KINK. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11474375 ↗

Other Tube, tracheal (w/wo connector) devices

All Tube, tracheal (w/wo connector) devices →

Sources and updates

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