Device recall
Z-0757-06: SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G
FDA device recall · Class II · Fischer Imaging Corporation
Key facts
| Recall number (Z-number) | Z-0757-06 |
|---|---|
| Recall event | 34975 |
| Product | SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G |
| Product code | MUE |
| Recalling firm | Fischer Imaging Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2012 |
| PMA numbers | P010017, P010017S007 |
| FEI number | 1418957 |
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