Device recall
Z-1017-2010: Dimension Vista System BUN Flex Reagent Cartridge, Catalog number K1021, in…
FDA device recall · Class II · Siemens Healthcare Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-1017-2010 |
|---|---|
| Recall event | 52958 |
| Product | Dimension Vista System BUN Flex Reagent Cartridge, Catalog number K1021, in vitro diagnostic. |
| Product code | JJE |
| Recalling firm | Siemens Healthcare Diagnostics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 30, 2010 |
| 510(k) numbers | K051087 |
| FEI number | 2517506 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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