Device recall
Z-0090-04: Device to determine quantitative total testosterone in human serum
FDA device recall · Class II · Qualigen Inc
Key facts
| Recall number (Z-number) | Z-0090-04 |
|---|---|
| Recall event | 27562 |
| Product | Device to determine quantitative total testosterone in human serum |
| Product code | CDZ |
| Recalling firm | Qualigen Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 30, 2004 |
| FEI number | 3003355251 |
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