Device recall
Z-2337-2015: Biograph 64-4R TruePoint w/ TrueV, Model Number 10097302
FDA device recall · Class II · Siemens Medical Solutions USA Inc.
Key facts
| Recall number (Z-number) | Z-2337-2015 |
|---|---|
| Recall event | 71712 |
| Product | Biograph 64-4R TruePoint w/ TrueV, Model Number 10097302 |
| Product code | KPS |
| Recalling firm | Siemens Medical Solutions USA Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 3, 2016 |
| 510(k) numbers | K123737 |
| FEI number | 1034973 |
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