Device recall
Z-0138-2009: Bicor Hi-P X-Ray System, Model numbers 6379767 and 6258383.
FDA device recall · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Recall number (Z-number) | Z-0138-2009 |
|---|---|
| Recall event | 49426 |
| Product | Bicor Hi-P X-Ray System, Model numbers 6379767 and 6258383. |
| Product code | IZI |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2012 |
| 510(k) numbers | K940484 |
| FEI number | 2240869 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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