Device recall
Z-1838-2023: Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125
FDA device recall · Class I · TELEFLEX LLC
Key facts
| Recall number (Z-number) | Z-1838-2023 |
|---|---|
| Recall event | 92373 |
| Product | Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125 |
| Product code | BTR |
| Recalling firm | TELEFLEX LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K780900 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 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