FDA Device recall Z-1922-2023
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055
- 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 100181055 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-1922-2023 |
| 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 100181055
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340573, Batch Numbers: 18FT35, 18GG18, 18GG23, 18GT32, 18IG16, 18JG35, 18KG01, 18KG39, 18LG15, 18LG18,…UDI/DI 14026704340573, Batch Numbers: 18FT35, 18GG18, 18GG23, 18GT32, 18IG16, 18JG35, 18KG01, 18KG39, 18LG15, 18LG18, 18LG39, 19AG01, 19AG25, 19CG02, 19CT33, 19DT05, 19DT35, 19ET36, 19ET61, 19ET65, 19KT02, 20AT26, 20CT11, 20DT19, KME21A2087, KME21B1774, KME21B2624, KME21B2710, KME21B2711, KME21C0549, KME22A0758, KME22A2298, KME22A2299, KME22B1465, KME22B1666, KME22B2680, KME22C2315, KME22C2316, KME22D1671, KME22D2352, KME22E1006, KME22E1007, KME22E1406, KME22E1930, KME22F2204, KME22F2482 |
|---|
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-1922-2023%22
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