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Mallinckrodt 126039Recalls & reported problems

Covidien LP · Endobronchial Suction Catheters with Color Coded Connectors; Endobronchial Tube; Endobronchial Tube Accessories,Right,(2) Right Angle Swivel Connectors; Carlens Y Adapter · Class 2

All models of Mallinckrodt (73)

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 30884522028978), received between May 9, 2019 and May 9, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Partial Blockage” (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

  • Partial Blockage1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 9, 2019Partial Blockage; Partial Blockage

    ACCORDING TO THE REPORTER, DURING INSPECTION BEFORE USE, AIR WAS INJECTED INTO THE CUFF, BUT THE CUFF COULD NOT BE DEFLATED. IT HAS NOT BEEN BENT FOR INTUBATION. THE STYLET WAS REMOVED, BUT IT COULD NOT BE DEFLATED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Patient Involvement

    MAUDE report 8595311 ↗

Other TUBE, BRONCHIAL (W/WO CONNECTOR) devices

All TUBE, BRONCHIAL (W/WO CONNECTOR) devices →

Sources and updates

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