Device recall
Z-1658-2016: Advia Chemistry Assay: Uric Acid and Uric Acid, concentrated
FDA device recall · Class II · Siemens Healthcare Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-1658-2016 |
|---|---|
| Recall event | 73667 |
| Product | Advia Chemistry Assay: Uric Acid and Uric Acid, concentrated |
| Product code | KNK |
| Recalling firm | Siemens Healthcare Diagnostics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 25, 2017 |
| 510(k) numbers | K991576 |
| FEI number | 2517506 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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