--- title: "Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cu... — FDA record Z-1952-2023 | Is It on Recall" description: "Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products." url: https://isitonrecall.com/recall/fda-device-z-1952-2023-preformed-agt-oral-endotracheal-tube-murphy-eye-high-volume-low-pressure-cuff-ref-111781050/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050 — FDA record Z-1952-2023 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date May 25, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050 - **Reason**: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. - **Classification**: Class I - **Recalling firm**: TELEFLEX LLC - **Quantity**: 302652 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-1952-2023 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1952-2023%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | UDI/DI 14026704341181, Batch Numbers: 18FG31, 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, 18HG17, 18HG19, 18HG21, 18HG22, 18HG29, 18IG15, 18IG17, 18IG30, 18JG16, 18JG19, 18JG35, 18JG37, 18KG17, 18KG39, 18KG40, 18LG14, 18LG15, 18LG18, 18LG39, 19AG25, 19BG02, 19BG04, 19BG18, 19BG19, 19BG32, 19CG01, 19CT28, 19CT33, 19CT36, 19CT56, 19CT57, 19CT80, 19DT05, 19DT30, 19ET34, 19ET36, 19ET39, 19ET40, 19ET61, 19ET65, 19FT01, 19FT45, 19GT13, 19GT63, 19HT24, 19HT31, 19HT53, 19IT54, 19JT06, 19JT10, 19JT11, 19JT14, 19JT35, 19JT63, 19KT14, 19KT38, 19KT41, 19KT46, 19LT17, 19LT21, 20AT22, 20BT53, 20CT07, 20CT12, 20CT14, 20CT32, 20DT18, 20DT29, 20ET34, 20ET38, 20ET49, 20FT17, 20FT19, 20FT21, 20FT64, 20GT11, KME20J0370, KME20J0663, KME20J0665, KME20J1212, KME20K3628, KME20L2213, KME20L2286, KME20L2666, KME20L2668, KME20M0644, KME20M1284, KME20M2643, KME20M2645, KME20M2956, KME20M3015, KME21A1024, KME21A1065, KME21A1273, KME21A2079, KME21A2235, KME21A3066, KME21B0255, KME21B0256, KME21B0378, KME21B2209, KME21B2274, KME21B2275, KME21B2535, KME21C0433, KME21C0643, KME21C1123, KME21C1125, KME21C1164, KME21E0006, KME21F0902, KME21F1216, KME21F2139, KME21F2198, KME21J0892, KME21J1496, KME21J1690, KME21J1813, KME21J2074, KME21K0004, KME21K0115, KME21K0296, KME21K0875, KME21K0877, KME21K1029, KME21K1079, KME21K1716, KME21K1826, KME21K1868, KME21K2303, KME21K2335, KME21K3007, KME21L0889, KME21L0985, KME21L1526, KME21L1597, KME21L1776, KME21L2153, KME21L2154, KME21L2299, KME21L2885, KME21M0162, KME21M0337, KME21M0342, KME21M0502, KME21M0733, KME21M0951, KME21M1978, KME21M1979, KME21M2427, KME21M2675, KME21M2676, KME21M2711, KME21M2807, KME22A0564, KME22A0565, KME22A1888, KME22A2257, KME22A2369, KME22A2370, KME22A2850, KME22A2919, KME22A2970, KME22B0006, KME22B0174, KME22B0360, KME22B0400, KME22B0665, KME22B0754, KME22B2315, KME22B2554, KME22B2557, KME22B2631, KME22B2633, KME22B2635, KME22B2678, KME22B2793, KME22B2794, KME22B2920, KME22C0553, KME22C1122, KME22C3230, KME22C3394, KME22C3396, KME22D0097, KME22D0108, KME22D0244, KME22D0286, KME22D0322, KME22D0538, KME22D0539, KME22D0602, KME22D0805, KME22D0854, KME22D0936, KME22D1008, KME22D1453, KME22D1957, KME22D2058, KME22D2293, KME22D2643, KME22D2765, KME22D3013, KME22E0947, KME22E0956, KME22E1500, KME22E1885, KME22E2219, KME22E2220, KME22E2440, KME22E2512, KME22E2872, KME22F0074, KME22F0542, KME22F0987, KME22F1112, KME22F2173, KME22F2206 | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution US Nationwide distribution including Puerto Rico. States below are derived from the distribution text, including nationwide wording. 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These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1952-2023%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [TELEFLEX LLC records](https://isitonrecall.com/brand/teleflex-llc/)