Sheridan Endotracheal Tube contained inside Centurion kit code TC7855 — Class I medical device recall Z-1956-2019
Terminated recall by Centurion Medical Products Corporation, reported 2019-08-07, distributed in AR. Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increase
| Recall number | Z-1956-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2019-06-07 |
| Classified | 2019-07-30 |
| Reported by FDA | 2019-08-07 |
| Terminated | 2020-07-28 |
| Distributed | AR |
| Quantity | 80 kits |
| Lot numbers | 2018110290 |
Product
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1956-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.