Device recall
Z-0996-04: Tecan clinical workstation; Tecan Genesis 150 front end, Roche catalog number…
FDA device recall · Class I · Roche Diagnostics Corp.
Key facts
| Recall number (Z-number) | Z-0996-04 |
|---|---|
| Recall event | 28984 |
| Product | Tecan clinical workstation; Tecan Genesis 150 front end, Roche catalog number 03585379001. |
| Product code | JQW |
| Recalling firm | Roche Diagnostics Corp. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 7, 2007 |
| 510(k) numbers | K953345 |
| 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