Device recall
Z-1355-2014: Syphilis Test Card (Serum); LumiQuick. Santa Clara, CA 95054
FDA device recall · Class II · LumiQuick Diagnostics Inc.
Key facts
| Recall number (Z-number) | Z-1355-2014 |
|---|---|
| Recall event | 67665 |
| Product | Syphilis Test Card (Serum); LumiQuick. Santa Clara, CA 95054 |
| Recalling firm | LumiQuick Diagnostics Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 9, 2014 |
| FEI number | 3005984081 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
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