Preformed AGT Oral Endotracheal Tube Murphy Eye recall
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050
Why was Preformed AGT Oral Endotracheal Tube Murphy Eye recalled?
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
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
- Product
- Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050
- Recalling firm
- TELEFLEX LLC
- Quantity
- 302652 units
- Distribution
- US Nationwide distribution including Puerto Rico.
- Recall date
- July 5, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)