Device recall
Z-1012-2023: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal…
FDA device recall · Class II · TELEFLEX LLC
Key facts
| Recall number (Z-number) | Z-1012-2023 |
|---|---|
| Recall event | 91301 |
| Product | Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff; b. Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff; c. Flexiset Super Safety Clear Tracheal Tube, oral/nasal with Cuff and Insertion Aid; d. RUSCHELIT Safety… |
| Product code | BTR |
| Recalling firm | TELEFLEX LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3005747797 |
At a glance
- None 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