Device recall
Z-1054-2015: Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to…
FDA device recall · Class II · Cardinal Health
Key facts
| Recall number (Z-number) | Z-1054-2015 |
|---|---|
| Recall event | 70185 |
| Product | Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical emergency facilities. Primarily used on infants and pediatric patients. |
| Product code | BSR |
| Recalling firm | Cardinal Health |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2016 |
| FEI number | 3001236905 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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