Teleflex Medical: Medical Device Recall in 2019 - (Recall #: Z-0703-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The Sheridan Endobronchial tube is indicated for main stem bronchus intubation and allows for selective inflation or deflation of either lung.

Product Classification:

Class II

Date Initiated: October 30, 2019

Date Posted: December 25, 2019

Recall Number: Z-0703-2020

Event ID: 84298

Reason for Recall:

The tracheal and brochial swivel connectors are incorrectly labeled.

Status: Terminated

Product Quantity: 53 units

Code Information:

Catalog: 5-16135; Manufacturing Lot: 73G1600257

Distribution Pattern:

US Nationwide distribution in the states of CT, OK, LA, IL, GA, NY, CA, MT, MI, MA, FL.

Voluntary or Mandated:

Voluntary: Firm initiated