Drug recall
HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial…
FDA recall event 84298 · Class II · Teleflex Medical
Key facts
| Event ID | 84298 |
|---|---|
| Recall numbers | Z-0703-2020 |
| Recalling firm | Teleflex Medical |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The tracheal and brochial swivel connectors are incorrectly labeled. |
| Initiation date | Oct 30, 2019 |
| Report date | Dec 25, 2019 |
| Termination date | Sep 30, 2021 |
| City | Morrisville |
| State | NC |
| Country | United States |
| FEI number | 3005747797 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: