Centurion Medical Products Corporation recalls Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.

Recall date

June 7, 2019

Source

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

Recall number

Z-1956-2019

FDA classification

Class I

Brand / firm

Centurion Medical Products Corporation

Sold / distributed

Distributed to one account in Arkansas.

Why it was recalled

Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.

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

Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.