FDA Device recall Z-1935-2023
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382040
- 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 100382040 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-1935-2023 |
| 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 100382040
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340818, Batch Numbers: 18FG31, 18FG33, 18FT13, 18GG15, 18HG08, 18HG10, 18HG25, 18IG13, 18JG08, 18KG09,…UDI/DI 14026704340818, Batch Numbers: 18FG31, 18FG33, 18FT13, 18GG15, 18HG08, 18HG10, 18HG25, 18IG13, 18JG08, 18KG09, 18KG33, 18LG01, 19BG12, 19BG35, 19ET09, 19FT12, 19GT05, 19IT11, 19KT20, 19KT38, 20AT37, 20CT12, 20CT53, 20DT04, 20ET56, 20FT21, 20FT43, 20GT18, KME20G0126, KME20H0286, KME20H1091, KME20H2041, KME20J2613, KME20K0326, KME20K0601, KME20M0209, KME20M1518, KME21B1133, KME21B1830, KME21C1573, KME21C1675, KME21C2245, KME21C3124, KME21D0525, KME21J0629, KME21K0797, KME21L2516, KME21L2526, KME21M0868, KME22C2637, KME22D0032, KME22D0811, KME22D0943, KME22D1009, KME22E0606, KME22E1274, KME22E2288 |
|---|
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-1935-2023%22
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