RecallRadar

FDA Device recall Z-1941-2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040

On 2023-07-05 the FDA classified a Class I recall of Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040 by Teleflex, citing reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1941-2023
ClassificationClass I
Statusongoing
Initiated2023-05-25
Published2023-07-05
Last updated2026-09-13 11:56 UTC
CompanyTeleflex
DistributionUS

Product

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040

Reason

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Identifiers

code_info
UDI/DI 14026704341044, Batch Numbers: 18FG24, 18GG03, 18GG04, 18GG24, 18GT26, 18HG24, 18JG07, 18KG22, 18KG34, 18LG33,…UDI/DI 14026704341044, Batch Numbers: 18FG24, 18GG03, 18GG04, 18GG24, 18GT26, 18HG24, 18JG07, 18KG22, 18KG34, 18LG33, 19AG36, 19BG12, 19CG07, 19CT69, 19DT42, 19ET58, 19FT18, 19GT43, 19GT44, 19JT55, 19KT38, 19LT32, 20AT09, 20AT49, 20BT53, 20DT24, 20ET50, 20FT36, 20FT60, 20GT40, KME21C0405, KME21C1057, KME22C0550, KME22C0648, KME22C1816, KME22C2806, KME22D1073, KME22D2150, KME22E0683, KME22E0684, KME22E2814, KME22E2897, KME22F1760, KME22F2739, KME22G0790, KME22H1304, KME22H2878, KME22J1447, KME22K0482, KME23A1241, KME23A2001, KME23A2181, KME23A2683, KME23A3032

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1941-2023%22

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