Device recall
Z-0799-2015: Sheridan/CF Cuffed Tracheal Tube, Sterile, Rx only, Teleflex Medical, Research…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0799-2015 |
|---|---|
| Recall event | 69758 |
| Product | Sheridan/CF Cuffed Tracheal Tube, Sterile, Rx only, Teleflex Medical, Research Triangle Park, NC 27708. Designed for oral and nasal intubation and are indicated for airway management. |
| Product code | BTR |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2017 |
| 510(k) numbers | K822082 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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