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Shiley 126041Recalls & reported problems

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

All models of Shiley (387)

Data updated Oct 16, 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 20884522028933), received between Mar 22, 2023 and Mar 22, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device 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

  • Use of Device Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionMar 22, 2023Use of Device Problem; Use of Device Problem

    ACCORDING TO THE REPORTER, THE BLUE AND REGULAR CUFFS OF BOTH DEVICES DID NOT INFLATE AND DEFLATE WHEN TESTED BEFORE USE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16594764 ↗

Other TUBE, BRONCHIAL (W/WO CONNECTOR) devices

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

Sources and updates

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