Device recall
Z-2881-2011: Calloway LabsMulti-Drug 9 Panel Assay A rapid, one step screening test for the…
FDA device recall · Class II · Alere San Diego
Key facts
| Recall number (Z-number) | Z-2881-2011 |
|---|---|
| Recall event | 59101 |
| Product | Calloway LabsMulti-Drug 9 Panel Assay A rapid, one step screening test for the simultaneous for the qualitative detection of multiple drugs and drug metabolites in human urine. |
| Product code | DKZ |
| Recalling firm | Alere San Diego |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 4, 2012 |
| 510(k) numbers | K061718 |
| FEI number | 1000125596 |
At a glance
- 1–9 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