FDA Device recall Z-1925-2023
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380025
- 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 100380025 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-1925-2023 |
| 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 100380025
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340610, Batch Numbers: 19ET51, 19FT29, 19GT05, 19GT35, 19HT79, 19JT51, 19KT06, 19LT28, 20AT05, 20AT37,…UDI/DI 14026704340610, Batch Numbers: 19ET51, 19FT29, 19GT05, 19GT35, 19HT79, 19JT51, 19KT06, 19LT28, 20AT05, 20AT37, 20AT54, 20BG15, 20DT24, 20ET03, KME21B0529, KME21C0887, KME21D0327, KME21F0137, KME21K0799, KME21K0800, KME22A2704, KME22C0981, KME22C1568, KME22D0029, KME22H0686, KME22H1360 |
|---|
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-1925-2023%22
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