FDA Device recall Z-1863-2023
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040
- 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 100180040 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-1863-2023 |
| 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 100180040
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340450, Batch Numbers: 18GT26, 18KG10, 18LG33, 19AG21, 19BG12, 19CT36, 19DT42, 19FT29, 19FT49, 20DT24,…UDI/DI 14026704340450, Batch Numbers: 18GT26, 18KG10, 18LG33, 19AG21, 19BG12, 19CT36, 19DT42, 19FT29, 19FT49, 20DT24, KME20L2493, KME20M0278, KME21A0061, KME21B1925, KME21M1736, KME22C0700, KME22F0734, KME22G0184, KME22H0033, KME22H3078, KME22J0843 |
|---|
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-1863-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.