Device recall
Z-1701-2014: Hologic M-IV Mammography System; Model M4--00001. Intended to produce…
FDA device recall · Class II · Hologic, Inc.
Key facts
| Recall number (Z-number) | Z-1701-2014 |
|---|---|
| Recall event | 68298 |
| Product | Hologic M-IV Mammography System; Model M4--00001. Intended to produce radiographic images of the breast. For screening and diagnostic imaging of the breast. |
| Product code | IZH |
| Recalling firm | Hologic, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2014 |
| 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