Medline Industries, Inc. DYND43080Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196726332), received between Sep 17, 2026 and Sep 29, 2026 — classified as 2 malfunctions.

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

1 other recall cover devices cleared under the same FDA submission (K042683); 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Sharp Edges

  It was reported that ¿hard sharp end of endotracheal tube.¿

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 50931634 ↗
• MalfunctionSep 17, 2026Inflation Problem

  It was reported that they had to put 80+cch2o into the cuff in order to inflate it.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50803591 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042683. One submission often covers many models, so check the product and lot details in each record.

• Z-3172-2026 · Jul 31, 2026 · Open, Classified
  SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25