Device recall
Z-1045-05: Mammomat Novation Digital Mammography System. Model number 6646900
FDA device recall · Class III · Siemens Medical Solutions USA, Inc
Key facts
| Recall number (Z-number) | Z-1045-05 |
|---|---|
| Recall event | 32515 |
| Product | Mammomat Novation Digital Mammography System. Model number 6646900 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 30, 2006 |
| PMA numbers | P030010 |
| FEI number | 2240869 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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