RecallRadar

FDA Device recall Z-1759-2019

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

On 2019-06-26 the FDA classified a Class I recall of Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management by Teleflex Medical, citing 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 Sh….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1759-2019
ClassificationClass I
Statusterminated
Initiated2019-05-24
Published2019-06-26
Last updated2026-09-13 11:55 UTC
CompanyTeleflex Medical
DistributionUS

Product

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

Reason

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.

Identifiers

code_info
Lot Numbers: 73K1600369, 73L1600011, 73A1700646, 73C1700238, 73D1700625, 73E1700475, 73F1700387, 73H1700041, 73H170048…Lot Numbers: 73K1600369, 73L1600011, 73A1700646, 73C1700238, 73D1700625, 73E1700475, 73F1700387, 73H1700041, 73H1700483, 73J1700292, 73L1700503, 73M1700453, 73A1800671, 73B1800350, 73D1800138, 73F1800174, 73G1800126, 73G1800806, 73J1800308, 73K1800173, 73L1800225, 73K1800172

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1759-2019%22

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