Device recall
Z-0672-05: Software written for a specific automated microtiter plate instrument, Bio-Tek…
FDA device recall · Class III · Diasorin Inc.
Key facts
| Recall number (Z-number) | Z-0672-05 |
|---|---|
| Recall event | 30920 |
| Product | Software written for a specific automated microtiter plate instrument, Bio-Tek ELx800 reader for use with the ENA 6 Screen ELISA kit assay. |
| Product code | LLL |
| Recalling firm | Diasorin Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 22, 2006 |
| 510(k) numbers | K944505 |
| FEI number | 2182595 |
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