Device recall
Z-2329-2008: SoftPath GUI Release Software Versions 3.17 and 4.1. Used in pathology…
FDA device recall · Class II · SCC Soft Computer
Key facts
| Recall number (Z-number) | Z-2329-2008 |
|---|---|
| Recall event | 35369 |
| Product | SoftPath GUI Release Software Versions 3.17 and 4.1. Used in pathology laboratory for receiving accessing specimen reports, billing and management reports for surgical, GYN, NON-GYN and Autopsy cases. |
| Product code | JQP |
| Recalling firm | SCC Soft Computer |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 20, 2008 |
| FEI number | 1000307651 |
At a glance
- None 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