Preformed AGT Oral Endotracheal Tube Murphy Eye — Class I medical device recall Z-1941-2023
Ongoing recall by TELEFLEX LLC, reported 2023-07-05, distributed nationwide. Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
| Recall number | Z-1941-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX LLC, Morrisville, NC, United States |
| Recall initiated | 2023-05-25 |
| Classified | 2023-06-29 |
| Reported by FDA | 2023-07-05 |
| Distributed | Nationwide (US) |
| Quantity | 20,042 units |
| UPC / GTIN / UDI-DI | 14026704341044 |
| Lot 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 and 14 more |
| Model numbers | 111780040 |
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040
Reason for recall
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.