FDA Device recall Z-1956-2019
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855
- FDA Device
- Class I
- terminated
- Published 2019-08-07
On 2019-08-07 the FDA classified a Class I recall of Sheridan Endotracheal Tube contained inside Centurion kit code TC7855 by Centurion Medical Products, citing centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotrac….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1956-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2019-06-07 |
| Published | 2019-08-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Centurion Medical Products |
| Distribution | AR |
Product
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
Reason
Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.
Identifiers
| code_info | Lot 2018110290 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1956-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.