--- title: "Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cu... — FDA record Z-1879-2023 | 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-1879-2023-preformed-agt-oral-endotracheal-tube-murphy-eye-high-volume-low-pressure-cuff-ref-111781045/ 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 111781045 — FDA record Z-1879-2023 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 111781045 - **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**: 446163 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-1879-2023 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1879-2023%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 14026704341174, Batch Numbers: 18FG33, 18GG16, 18HG17, 18HG21, 18HG29, 18HG30, 18HG31, 18IG10, 18IG14, 18IG17, 18IG20, 18JG02, 18JG03, 18JG16, 18JG19, 18JG20, 18JG35, 18JG37, 18KG01, 18KG17, 18KG19, 18KG36, 18KG39, 18KG41, 18LG12, 18LG14, 18LG30, 18LG39, 19AG01, 19AG17, 19AG19, 19AG29, 19BG02, 19BG18, 19BG19, 19BG32, 19BG33, 19CG01, 19CT26, 19CT33, 19CT53, 19CT56, 19CT80, 19DT05, 19DT30, 19DT46, 19ET18, 19ET34, 19ET39, 19ET40, 19ET61, 19ET65, 19ET69, 19FT01, 19FT41, 19GT13, 19HT68, 19IT01, 19IT15, 19IT53, 19IT54, 19JT06, 19JT10, 19JT14, 19JT56, 19JT63, 19KT02, 19KT14, 19KT38, 19KT41, 19LT16, 19LT21, 19LT36, 20AT22, 20BT02, 20CT02, 20CT05, 20CT11, 20CT14, 20CT32, 20DT19, 20DT20, 20DT23, 20DT29, 20DT32, 20DT35, 20ET33, 20ET34, 20ET38, 20ET39, 20ET49, 20FT17, 20FT18, 20FT60, 20GT34, KME20H0612, KME20H1787, KME20H2570, KME20H2572, KME20H2573, KME20H3001, KME20H3127, KME20H3128, KME20J1211, KME20J1389, KME21A1007, KME21A1008, KME21A1182, KME21A2025, KME21A2026, KME21A2189, KME21A3059, KME21A3060, KME21A3083, KME21A3084, KME21B0258, KME21B0790, KME21B1083, KME21B1259, KME21B1289, KME21B1545, KME21B1605, KME21B1754, KME21B2217, KME21B2530, KME21B2672, KME21C0424, KME21C0425, KME21C2416, KME21J1495, KME21K1633, KME21K1715, KME21K1842, KME21K1866, KME21K2302, KME21K2458, KME21K2459, KME21K2495, KME21K2579, KME21K2998, KME21K3000, KME21K3001, KME21L0074, KME21L0890, KME21L1033, KME21L1359, KME21L1364, KME21L1365, KME21L1435, KME21L1525, KME21L2143, KME21L2788, KME21M0949, KME21M1654, KME21M1655, KME21M1656, KME21M1906, KME21M1907, KME21M2271, KME21M2424, KME21M2479, KME21M2674, KME21M2706, KME21M2909, KME22A0562, KME22A1471, KME22A2179, KME22A2917, KME22A3198, KME22A3264, KME22B0005, KME22B0167, KME22B0191, KME22B0239, KME22B0277, KME22B0358, KME22B0399, KME22B0502, KME22B0580, KME22B1038, KME22B1144, KME22B1145, KME22B1224, KME22B1265, KME22B1309, KME22B1341, KME22B1418, KME22C0060, KME22C0494, KME22C0791, KME22C0792, KME22C1080, KME22C1081, KME22C1082, KME22C1236, KME22C1237, KME22C1472, KME22C1710, KME22C1711, KME22C1724, KME22C1850, KME22C1852, KME22C1878, KME22C1879, KME22C1880, KME22C1991, KME22C1992, KME22C2190, KME22C2968, KME22D0091, KME22D0153, KME22D0248, KME22D0285, KME22D0321, KME22D0444, KME22D0536, KME22D0717, KME22D1659, KME22D2057, KME22D2469, KME22D3211, KME22E1501, KME22E1932, KME22E2026, KME22E2122, KME22E2690, KME22E2805, KME22E2888, KME22E2928, KME22F0230, KME22F2072, KME22F2355, KME22F2625, KME22F3383, KME22F3502, KME22G0215, KME22G0234, KME22G0262, KME22G0476, KME22G0537, KME22G0735, KME22G0788, KME22G1047, KME22G1109, KME22G1332, KME22G1466, KME22G2049, KME22G2244, KME22G2774, KME22H1202 | 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-1879-2023%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [TELEFLEX LLC records](https://isitonrecall.com/brand/teleflex-llc/)