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Bivona FT21CN65NSC054NRecalls & reported problems

Icu Medical, Inc. · Class 2

All models of Bivona (469)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 15019517260434), received between Jun 6, 2022 and Jun 15, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Inflation Problem” (3 reports).

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

Device problems

  • Inflation Problem3

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 15, 2022Inflation Problem; Inflation Problem

    IT WAS REPORTED THAT THE TRACH WOULD NOT INFLATE. THIS EVENT WAS DISCOVERED DURING TESTING PRIOR TO USE. NO PATIENT WAS INVOLVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14696780 ↗
  • MalfunctionJun 6, 2022Inflation Problem; Inflation Problem

    IT WAS REPORTED THAT THE DEVICE WOULD NOT INFLATE ALL THE WAY. THIS WAS DISCOVERED PRIOR TO PATIENT USE, AND THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14602982 ↗
  • MalfunctionJun 6, 2022Inflation Problem; Inflation Problem

    IT WAS REPORTED THAT THE DEVICE WOULD NOT INFLATE ALL THE WAY. THIS WAS DISCOVERED PRIOR TO PATIENT USE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14602764 ↗

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.

Other Tube tracheostomy and tube cuff devices

All Tube tracheostomy and tube cuff devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page