Device recall
Z-1865-2016: The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-1865-2016 |
|---|---|
| Recall event | 73826 |
| Product | The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic steroid, in plasma. |
| Product code | CHP |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 11, 2018 |
| FEI number | 1415939 |
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