FDA Device recall Z-1844-2023
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155
- FDA Device
- Class I
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class I recall of Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155 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-1844-2023 |
| 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
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704644947, Batch Numbers: 18JG17, 19AG37, 19CT32, 19ET22, 19ET38, 19ET60, 19IT54, 20AT32, 20CT22, 20DT29,…UDI/DI 14026704644947, Batch Numbers: 18JG17, 19AG37, 19CT32, 19ET22, 19ET38, 19ET60, 19IT54, 20AT32, 20CT22, 20DT29, KME20G0385, KME20K2550, KME20L1492, KME20M0813, KME21A2775, KME21B1698, KME21C2646, KME21J0882, KME21J0883, KME22F0239, KME22F0718, KME22F2420, KME22J0254, KME22J0262, KME22K2780 |
|---|
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-1844-2023%22
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