Drug recall
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly…
FDA recall event 67630 · Class II · Teleflex Medical
Key facts
| Event ID | 67630 |
|---|---|
| Recall numbers | Z-1231-2014 |
| Recalling firm | Teleflex Medical |
| Product type | Devices |
| Products | Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated with oral endobronchial tubes, including, but not limited to, thoracic surgery… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The product may fail to achieve seal of right lung due to the cuff inflating to one side |
| Initiation date | Feb 28, 2014 |
| Report date | Mar 26, 2014 |
| Termination date | Sep 28, 2016 |
| City | Durham |
| 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: