Device recall
Z-0574-05: BioTek brand Automated Microplate Reader; model ELx808, Roche catalog number…
FDA device recall · Class II · Roche Diagnostics Corp.
Key facts
| Recall number (Z-number) | Z-0574-05 |
|---|---|
| Recall event | 31146 |
| Product | BioTek brand Automated Microplate Reader; model ELx808, Roche catalog number 03145387001. |
| Product code | JJQ |
| Recalling firm | Roche Diagnostics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 10, 2006 |
| 510(k) numbers | K953710 |
| FEI number | 1823260 |
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