FDA Device recall Z-1898-2023
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040
- FDA Device
- Class I
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class I recall of RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040 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-1898-2023 |
| 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
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704341525, Batch Numbers: 18FG14, 18FG22, 18JG08, 18KG25, 18LG04, 18LG30, 19DT35, 19DT36, 19ET09, 19ET31,…UDI/DI 14026704341525, Batch Numbers: 18FG14, 18FG22, 18JG08, 18KG25, 18LG04, 18LG30, 19DT35, 19DT36, 19ET09, 19ET31, 19ET51, 19HT60, 19IT32, 19IT43, 20AT06, 20AT39, 20BT01, 20BT53, 20CT12, 20CT27, 20CT54, 20DT04, 20ET30, 20FT58, KME20G0182, KME20H0372, KME20H0373, KME20J0924, KME20J2043, KME21C2368, KME21K1187, KME21K1188, KME21K1977, KME21M1084, KME21M1842, KME21M1845, KME21M2733, KME21M2734, KME21M2735, KME21M2736, KME22B2019, KME22C1693, KME22D0057, KME22D0180, KME22D0819, KME22D1066, KME22D3269, KME22E0602, KME22E2648, KME22E2681, KME22F1440, KME22F1692, KME22F2455, KME22G2312, KME22H1126, KME22H1212, KME22H2302, KME22J1615, KME22K0283, KME22K0632, KME22K1096, KME22M1155, KME22M1478, KME22M1659, KME23B3174 |
|---|
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-1898-2023%22
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