Device recall
Z-0355-2012: SoftPath GUI Versions: 4.3.0.10, 4.3.0.11, and 4.3.0.12. SoftPath is a…
FDA device recall · Class II · SCC Soft Computer
Key facts
| Recall number (Z-number) | Z-0355-2012 |
|---|---|
| Recall event | 60451 |
| Product | SoftPath GUI Versions: 4.3.0.10, 4.3.0.11, and 4.3.0.12. SoftPath is a laboratory information system to be used in a clinical laboratory by knowledgeable, trained, and experienced personnel. SoftPath enables the user to document steps in the receiving and processing of surgical, gynecological… |
| Product code | LNX |
| Recalling firm | SCC Soft Computer |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2012 |
| FEI number | 1000307651 |
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