FDA Device recall Z-1937-2023
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055
- 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 100382055 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-1937-2023 |
| 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 100382055
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340849, Batch Numbers: 18FG21, 18FG33, 18FT17, 18FT31, 18GT06, 18HG06, 18HG15, 18IT06, 18JG14, 18JT12,…UDI/DI 14026704340849, Batch Numbers: 18FG21, 18FG33, 18FT17, 18FT31, 18GT06, 18HG06, 18HG15, 18IT06, 18JG14, 18JT12, 18KG10, 19AG05, 19AT23, 19BG10, 19BG21, 19BG26, 19BT08, 20CT47, 20DT01, 20GG45, 20GT40, KME20H0294, KME20H3036, KME20J0600, KME20J2166, KME20K1116, KME20K1206, KME20K3277, KME20L1040, KME20L1224, KME22F2548 |
|---|
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-1937-2023%22
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