Device recall
Z-0999-04: Tecan clinical workstation; 10-410 Tecan Genesis 150 back end, Roche catalog…
FDA device recall · Class I · Roche Diagnostics Corp.
Key facts
| Recall number (Z-number) | Z-0999-04 |
|---|---|
| Recall event | 29060 |
| Product | Tecan clinical workstation; 10-410 Tecan Genesis 150 back end, Roche catalog number 03585352001. |
| Product code | JQW |
| Recalling firm | Roche Diagnostics Corp. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 24, 2007 |
| FEI number | 1823260 |
At a glance
- None 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