Device recall
Z-0102-2011: SoftPath GUI version 4.2.3.4 2008-06-30 (Manuf Date). SoftPath GUI version…
FDA device recall · Class II · SCC Soft Computer
Key facts
| Recall number (Z-number) | Z-0102-2011 |
|---|---|
| Recall event | 56272 |
| Product | SoftPath GUI version 4.2.3.4 2008-06-30 (Manuf Date). SoftPath GUI version 4.2.4.1 2008-09-30 (Manuf Date). SoftPath GUI version 4.3.0.3, 2008-07-23 (Manuf Date). SoftPath GUI version 4.3.0.4 2008-09-16 (Manuf Date). SCC Soft Computer, 5400 Tech Data Drive, Clearwater, FL 33760. |
| Product code | LNX |
| Recalling firm | SCC Soft Computer |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2010 |
| 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