FDA Device recall Z-1837-2023
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120
- 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 170120 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-1837-2023 |
| 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 170120
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704644879, Batch Numbers: 18JG23, 18JG26, 18JG34, 18KG26, 18LG05, 19AG18, 19AG21, 19AG24, 19AG37, 19BG01,…UDI/DI 14026704644879, Batch Numbers: 18JG23, 18JG26, 18JG34, 18KG26, 18LG05, 19AG18, 19AG21, 19AG24, 19AG37, 19BG01, 19BG04, 19BG07, 19BG12, 19BG16, 19CT58, 19CT71, 19DT06, 19DT20, 19ET77, 19FT14, KME20H0975, KME20H0976, KME20J0324, KME20K0771, KME20K2545, KME20K2568, KME20L0627, KME21A1886, KME21B1671, KME21B2506, KME21C2475, KME21D0447, KME21K1723, KME22A0056, KME22B0179, KME22B0180, KME22B0181, KME22B0464, KME22C2255, KME22C2256, KME22D1638, KME22D1639, KME22D1788, KME22E1489, KME22F1500, KME22F1669, KME22F1670, KME22G3099, KME22H3107, KME22H3275, KME22J2354, KME22J2355, KME22J2356, KME23A2360 |
|---|
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-1837-2023%22
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