Device recall
Z-2453-2012: Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version 5.0.1and…
FDA device recall · Class II · Hologic, Inc.
Key facts
| Recall number (Z-number) | Z-2453-2012 |
|---|---|
| Recall event | 63180 |
| Product | Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version 5.0.1and 5.0.2 The device is a Mini C-arm Fluoroscopic Imaging System designed to provide -physicians with general fluoroscopic visualization of a patient, including but not limited to surgical orthopedic and podiatry use… |
| Product code | JAA |
| Recalling firm | Hologic, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 10, 2014 |
| 510(k) numbers | K051025 |
| FEI number | 1221300 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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