FDA recall Z-1956-2019

Product

Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.

Reason for recall

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.

Distribution

Distributed to one account in Arkansas.

Key facts

Status

Terminated

Initiation date

2019-06-07

Report date

2019-08-07

Termination date

2020-07-28

Voluntary/Mandated

Voluntary: Firm initiated

Location

Williamston, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1956-2019