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Halyard 35161Recalls & reported problems

Avanos Medical, Inc. · ENDOTRACHEAL TUBE PEDIATRIC ORAL CURVED 3.MM · Class 2

All models of Halyard (232)

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 10680651351613), received between Jan 9, 2023 and Jan 9, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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

  • Loose or Intermittent Connection1
  • Patient Device Interaction 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.

  • MalfunctionJan 9, 2023Loose or Intermittent Connection; Patient Device Interaction Problem

    PATIENT IS INTUBATED WITH A 3.0 ETT, TUBE IS SECURE, SEDATION IS ADEQUATE, HOWEVER ANY SLIGHT MOVEMENT OR COUGH CAUSES THE BLUE PIECE OF ETT TO POP OF THE VENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16120867 ↗

Other Tube, Tracheal (W/Wo Connector) devices

All Tube, Tracheal (W/Wo Connector) devices →

Sources and updates

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