Device recall
Z-2884-2016: DRI Salicylate Serum Tox Assay, Catalog number 0977. Toxicology: The DRI…
FDA device recall · Class II · Microgenics Corporation
Key facts
| Recall number (Z-number) | Z-2884-2016 |
|---|---|
| Recall event | 74861 |
| Product | DRI Salicylate Serum Tox Assay, Catalog number 0977. Toxicology: The DRI Salicylate Serum Tox Assay is intended for the quantitative determination of salicylate in human serum or plasma. |
| Product code | DKJ |
| Recalling firm | Microgenics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2016 |
| 510(k) numbers | K961131 |
| FEI number | 3010939897 |
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