TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060

Recall date

May 25, 2023

Source

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

Recall number

Z-1945-2023

FDA classification

Class I

Brand / firm

TELEFLEX LLC

Sold / distributed

US Nationwide distribution including Puerto Rico.

Why it was recalled

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060