Bivona FT22LN40NSF858NRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15019517324747), received between Jan 23, 2023 and Jan 23, 2023 — classified as 1 malfunction.

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

• MalfunctionJan 23, 2023Inflation Problem; Inflation Problem

  IT WAS REPORTED THAT A TRACHEOSTOMY TUBE BALLOON DID NOT INFLATE WHEN WATER WAS ADDED, PRIOR TO PATIENT USE. THE TRACH WAS CHECKED PRIOR TO PLACEMENT AND THE ISSUE WAS DISCOVERED AT THAT TIME. NO HARM TO THE PATIENT OCCURRED. NO MEDICAL INTERVENTION WAS REQUIRED. THE EVENT WAS RESOLVED AS THE TRACH WAS NOT PLACED; ANOTHER PROPERLY FUNCTIONING TRACH WAS SUCCESSFULLY PLACED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16223627 ↗

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.