HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 — Class II medical device recall Z-0703-2020
Terminated recall by Teleflex Medical, reported 2019-12-25, distributed nationwide. The tracheal and brochial swivel connectors are incorrectly labeled.
| Recall number | Z-0703-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Morrisville, NC, United States |
| Recall initiated | 2019-10-30 |
| Classified | 2019-12-18 |
| Reported by FDA | 2019-12-25 |
| Terminated | 2021-09-30 |
| Distributed | Nationwide (US) |
| Quantity | 53 units |
| Reason classes | labeling |
| Lot numbers | 73G1600257 |
| Model numbers | 5-16135 |
Product
HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The Sheridan Endobronchial tube is indicated for main stem bronchus intubation and allows for selective inflation or deflation of either lung.
Reason for recall
The tracheal and brochial swivel connectors are incorrectly labeled.
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-0703-2020. 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.