Device recall
Z-1231-2014: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1231-2014 |
|---|---|
| Recall event | 67630 |
| Product | 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, bronchospirometry, administration of endobronchial anesthesia, etc. The endobronchial tube allows… |
| Product code | BTS |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 28, 2016 |
| 510(k) numbers | K951091 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database