FDA Device recall Z-1934-2023
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
- 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 - Murphy, REF 100382025 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-1934-2023 |
| 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 - Murphy, REF 100382025
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340788, Batch Numbers: 18FG22, 18FG31, 18FT13, 18GG16, 18GG34, 18GT12, 18HG08, 18IG13, 18IG14, 18JG09,…UDI/DI 14026704340788, Batch Numbers: 18FG22, 18FG31, 18FT13, 18GG16, 18GG34, 18GT12, 18HG08, 18IG13, 18IG14, 18JG09, 18JG14, 18JG35, 18KG08, 18LG15, 19AG04, 19AG07, 19AG21, 19BG12, 19CT37, 19CT41, 19CT44, 19CT64, 19ET57, 19FT25, 19GT04, 19GT29, 19KT65, 19LT03, 19LT27, 20AT37, 20BT15, 20CT12, 20DT04, 20ET03, 20ET33, 20FT21, 20FT40, 20GG41, KME20K2027, KME20K3208, KME21C1802, KME21C2684, KME21D0352, KME21D0601, KME21D1281, KME21D1818, KME21E1427, KME21M3077, KME22B1025, KME22B1089, KME22C0099, KME22E0297, KME22F0538, KME22F2559, KME22F2561, KME22G0176, KME22H1542, KME22K0062, KME22K0425, KME22K2437, KME22K2588, KME22L2985 |
|---|
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-1934-2023%22
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