Device recall
Z-0148-04: Lorad M-IV Mammography System
FDA device recall · Class II · Lorad, A Division of Hologic
Key facts
| Recall number (Z-number) | Z-0148-04 |
|---|---|
| Recall event | 29764 |
| Product | Lorad M-IV Mammography System |
| Product code | IZH |
| Recalling firm | Lorad, A Division of Hologic |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 15, 2004 |
| 510(k) numbers | K011987 |
| FEI number | 1220984 |
At a glance
- 1–9 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