Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management
- Company
- Teleflex Medical
- Recall Initiated
- May 24, 2019
- Posted
- June 19, 2019
- Terminated
- February 15, 2022
- Recall Number
- Z-1759-2019
- Quantity
- 3483 units
- Firm Location
- Morrisville, NC
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.
Distribution
Worldwide - US Nationwide Distribution
Lot / Code Info
Lot Numbers: 73K1600369, 73L1600011, 73A1700646, 73C1700238, 73D1700625, 73E1700475, 73F1700387, 73H1700041, 73H1700483, 73J1700292, 73L1700503, 73M1700453, 73A1800671, 73B1800350, 73D1800138, 73F1800174, 73G1800126, 73G1800806, 73J1800308, 73K1800173, 73L1800225, 73K1800172
Root Cause
Process control
Action Taken
Teleflex sent an Urgent Medical Device Recall letter dated May 24, 2019 to customers. The letter identified the affected product, problem and actions to be taken. The letter directed customers to discontinue use, quarantine the product, and contact Teleflex for return of the product. Distributors were directed to notify their customers and request the customer return the recalled products to them for consolidation and subsequent return to Teleflex.. For questions contact your local sales representative or Customer Service at 1-866-396-2111