FDA Device recall Z-0246-2016
Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical
- FDA Device
- Class II
- terminated
- Published 2015-11-18
On 2015-11-18 the FDA classified a Class II recall of Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical by Teleflex Medical, citing due to reports of the plastic coating of the stylet splitting and/or breaking off of the stylet.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0246-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-24 |
| Published | 2015-11-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| Distribution | US |
Product
Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.
Reason
Due to reports of the plastic coating of the stylet splitting and/or breaking off of the stylet.
Identifiers
| code_info | Material #503700-000060, Batch numbers: 13IG21, 13LG06, 14AG04, 14FG06, 14GG01, 14LG06, 15AG28, 15CG24 and 15DG38. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0246-2016%22
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