Teleflex Medical: Medical Device Recall in 2019 - (Recall #: Z-1759-2019)

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 LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management

Product Classification:

Class I

Date Initiated: May 24, 2019

Date Posted: June 26, 2019

Recall Number: Z-1759-2019

Event ID: 82964

Reason for Recall:

This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.

Status: Terminated

Product Quantity: 3483 units

Code Information:

Lot Numbers: 73K1600369, 73L1600011, 73A1700646, 73C1700238, 73D1700625, 73E1700475, 73F1700387, 73H1700041, 73H1700483, 73J1700292, 73L1700503, 73M1700453, 73A1800671, 73B1800350, 73D1800138, 73F1800174, 73G1800126, 73G1800806, 73J1800308, 73K1800173, 73L1800225, 73K1800172

Distribution Pattern:

Worldwide - US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated