FDA Device recall Z-1903-2023
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150035
- 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 150035 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-1903-2023 |
| 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 150035
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 4026704319671, Batch Numbers: 18FG15, 18GG12, 18GG14, 18JG02 |
|---|
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-1903-2023%22
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