FDA Device recall Z-1866-2023
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180055
- FDA Device
- Class I
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class I recall of Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180055 by Teleflex, citing reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1866-2023 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-05-25 |
| Published | 2023-07-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Teleflex |
| Distribution | US |
Product
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180055
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340481, Batch Numbers: 18IG24, 18JG36, 18LG33, 19AG11, 19AG21, 19DT06, 19ET58, 19FT22, 19FT49, 19HT04,…UDI/DI 14026704340481, Batch Numbers: 18IG24, 18JG36, 18LG33, 19AG11, 19AG21, 19DT06, 19ET58, 19FT22, 19FT49, 19HT04, 19HT34, 19HT80, 19IT43, 19JT02, 20AT49, 20BT53, 20CT24, 20DT24, 20GG27, KME20K2673, KME20M0950, KME21A0310, KME21B0602, KME22F0738 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1866-2023%22
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