Device recall
Z-1010-2023: Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for…
FDA device recall · Class II · TELEFLEX LLC
Key facts
| Recall number (Z-number) | Z-1010-2023 |
|---|---|
| Recall event | 91301 |
| Product | Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation |
| Product code | BTR |
| Recalling firm | TELEFLEX LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K780900 |
| 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