Device recall
Z-0467-2015: Calcitonin ELISA Kit, Code No. 7024, 7024BU. Intended use of this product is the…
FDA device recall · Class II · Biomerica
Key facts
| Recall number (Z-number) | Z-0467-2015 |
|---|---|
| Recall event | 69621 |
| Product | Calcitonin ELISA Kit, Code No. 7024, 7024BU. Intended use of this product is the quantitative determination of Calcitonin in human serum. |
| Product code | JKR |
| Recalling firm | Biomerica |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 28, 2015 |
| 510(k) numbers | K982491 |
| FEI number | 3007981058 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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