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Mallinckrodt 86552Recalls & reported problems

Covidien LP · Oral/Nasal Tracheal Tube Cuffed,Reinforced, Murphy Eye · Class 2

All models of Mallinckrodt (73)

Data updated Oct 16, 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 10884522043373), received between Mar 11, 2019 and Apr 2, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Inflation 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

  • Inflation Problem1
  • Material Split, Cut or Torn1

Patient problems

  • No Consequences Or Impact To Patient2

Recent adverse event reports

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

  • MalfunctionApr 2, 2019Inflation Problem; Inflation Problem

    ACCORDING TO THE REPORTER, THE DEVICE'S PILOT BALLOON HAD A DEFLATION/INFLATION ISSUE. THERE WAS NO PATIENT HARM.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8476255 ↗
  • MalfunctionMar 11, 2019Material Split, Cut or Torn; Material Split, Cut or Torn

    ACCORDING TO THE REPORTER, THE UNIT HAD POPPED OFF WITH EACH BREATHE. THERE WAS NO PATIENT HARM ASSOCIATED WITH THIS EVENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8409205 ↗

Other Tube, tracheal (w/wo connector) devices

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

Sources and updates

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