Preformed AGT Oral Endotracheal Tube Murphy Eye — Class I medical device recall Z-1949-2023
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-1949-2023 |
|---|---|
| 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 | 670 units |
| UPC / GTIN / UDI-DI | 14026704341136 |
| Lot numbers | 18GG25, 18LG18, 19AG19, 19DT36, 20CT32, 20GT34, KME21B2675, KME21F0887, KME22H1797 |
| Model numbers | 111780085 |
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780085
Reason for recall
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1949-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.