Hudson RCI Sheridan LTS recall
Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management
Why was Hudson RCI Sheridan LTS recalled?
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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: 73K1600369, 73L1600011, 73A1700646, 73C1700238, 73D1700625, 73E1700475, 73F1700387, 73H1700041, 73H1700483, 73J1700292, 73L1700503, 73M1700453, 73A1800671, 73B1800350, 73D1800138, 73F1800174, 73G1800126, 73G1800806, 73J1800308, 73K1800173, 73L1800225, 73K1800172
- Product
- Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management
- Recalling firm
- Teleflex Medical
- Quantity
- 3483 units
- Distribution
- Worldwide - US Nationwide Distribution
- Recall date
- June 26, 2019
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)