Device recall
Z-1124-2015: RSCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is…
FDA device recall · Class II · Teleflex, Inc.
Key facts
| Recall number (Z-number) | Z-1124-2015 |
|---|---|
| Recall event | 70087 |
| Product | RSCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following… |
| Product code | BTR |
| Recalling firm | Teleflex, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 30, 2015 |
| 510(k) numbers | K990619 |
| FEI number | 3011369183 |
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