Drug recall
Hudson RCI, Sheridan, Preformed Tracheal Tubes, Cuffed and Uncuffed, Rx Only, Sterile, Teleflex Medical.
FDA recall event 70248 · Class II · Teleflex Medical
Key facts
| Event ID | 70248 |
|---|---|
| Recall numbers | Z-1078-2015 |
| Recalling firm | Teleflex Medical |
| Product type | Devices |
| Products | Hudson RCI, Sheridan, Preformed Tracheal Tubes, Cuffed and Uncuffed, Rx Only, Sterile, Teleflex Medical. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Labeling; The affected product packaging is incorrectly labeled as being a cuffed oral ET tube; The correct product labeling is uncuffed nasal ET tube. |
| Initiation date | Jan 9, 2015 |
| Report date | Feb 18, 2015 |
| Termination date | Sep 27, 2016 |
| City | Research Triangle Park |
| State | NC |
| Country | United States |
| FEI number | 1044475 |
At a glance
- 1–9 Products in this recall
- None 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: