FDA Device recall Z-1882-2023
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095
- FDA Device
- Class I
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class I recall of Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095 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-1882-2023 |
| 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
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704341266, Batch Numbers: 18IT25, 18JG13, 19CT66, 19HT79, 19KT08, 20BT13, 20DT19, KME22C0673 |
|---|
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-1882-2023%22
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