FDA Device recall Z-1930-2023
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050
- FDA Device
- Class I
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class I recall of Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050 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-1930-2023 |
| 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
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340665, Batch Numbers: 18FG05, 18FT26, 18GT27, 18IG06, 18JG20, 18LG03, 18LT24, 19BG30, 19CT50, 19DT17,…UDI/DI 14026704340665, Batch Numbers: 18FG05, 18FT26, 18GT27, 18IG06, 18JG20, 18LG03, 18LT24, 19BG30, 19CT50, 19DT17, 19KT21, 19LT51, 20AT26, 20AT41, 20CT43, 20DT13, 20GG27, KME20H2359, KME20K1713, KME20L1811, KME20M2219, KME21A2253, KME21B0984, KME21L0988, KME22D2223, KME22D3339, KME22E0284, KME22F3118, KME22H2816 |
|---|
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-1930-2023%22
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