Device recall
Z-0708-05: Versa TREK REDOX 2 80 ml Anaerobic blood culture bottles, Product Code: 7103-44…
FDA device recall · Class III · Trek Diagnostic Systems
Key facts
| Recall number (Z-number) | Z-0708-05 |
|---|---|
| Recall event | 31375 |
| Product | Versa TREK REDOX 2 80 ml Anaerobic blood culture bottles, Product Code: 7103-44. The product was distributed in cases containing 50 bottles per case. |
| Product code | MDB |
| Recalling firm | Trek Diagnostic Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 28, 2005 |
| FEI number | 1000515493 |
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