FDA Device recall Z-1895-2023
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480025
- 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 112480025 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-1895-2023 |
| 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 112480025
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704341495, Batch Numbers: 18FG31, 18GT32, 18IG03, 18IG29, 18KG08, 18LG03, 19AG08, 19AG38, 19BG12, 19BG35,…UDI/DI 14026704341495, Batch Numbers: 18FG31, 18GT32, 18IG03, 18IG29, 18KG08, 18LG03, 19AG08, 19AG38, 19BG12, 19BG35, 19DT13, 19DT36, 19ET51, 19FT12, 19FT28, 19GT02, 19HT05, 19HT79, 19IT59, 19LT08, 19LT31, 20BG15, 20BT01, 20CT07, 20DT24, 20ET53, 20GT38, KME20H2416, KME20H2417, KME20J1068, KME20K2143, KME20K2598, KME20L0449, KME20L1346, KME20M0127, KME20M1797, KME21A0348, KME21B0087, KME21B0465, KME21C0163, KME21C1805, KME21C2447, KME21C2688, KME21C3244, KME21K2877, KME22A1408, KME22A2390, KME22A2545, KME22B0845, KME22B2017, KME22B2848, KME22C2802, KME22E0598, KME22E2130, KME22E2191, KME22G1878, KME22G2593, KME22H0532, KME22H1185, KME22H2178, KME22H2180, KME22J1309, KME22J2321 |
|---|
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-1895-2023%22
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