Device recall
Z-2713-2016: The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood…
FDA device recall · Class II · Cardinal Health
Key facts
| Recall number (Z-number) | Z-2713-2016 |
|---|---|
| Recall event | 74706 |
| Product | The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis. |
| Product code | CBT |
| Recalling firm | Cardinal Health |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 2, 2018 |
| 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