Bivona ST20GN40NGF026NRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15019517234886), received between Feb 4, 2022 and Feb 4, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

1 other recall cover devices cleared under the same FDA submission (K923878); they may or may not involve this specific model.

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

Recent adverse event reports

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

• InjuryFeb 4, 2022Break; Contamination; Break; Contamination

  IT WAS REPORTED THAT THE TRACH TUBE IN SITU WHEN INNER LUMEN NOTICED TO HAVE A MATERIAL?SIMILAR TO RADIO-OPAQUE LINE MIGRATING INTO AIRWAY. PATIENT VENTILATED FULL TIME AND WAS UNSTABLE AT THE TIME THE ISSUE WAS NOTICED. DUE TO HIGH-RISK PATIENT'S UNSTABLE AIRWAY, THE ENT CHANGED THE TUBE. NO INJURY OR IMPACT ON PATIENT STATUS OCCURRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13453576 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K923878. One submission often covers many models, so check the product and lot details in each record.

• Z-0260-2007 · Nov 17, 2006 · Terminated
  Custom 5.5 mm Bivona Uncuffed Hyperflex Tracheostomy Tube, I.D. 5.5 mm, O.D. 8.0 mm, length 4.75 mm, Mfrd by Smiths Medical Critical Care; REF HU05JS55NNA112S.