Medline Industries, LP recalls Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B

Recall date

December 24, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1313-2026

FDA classification

Class II

Brand / firm

Medline Industries, LP

Sold / distributed

Distribution US nationwide and Canada.

Why it was recalled

A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B