Device recall
Z-1243-2007: Cerner Millennium RadNet Auto Launch Study and Auto Launch Report software…
FDA device recall · Class II · Cerner Corp
Key facts
| Recall number (Z-number) | Z-1243-2007 |
|---|---|
| Recall event | 44739 |
| Product | Cerner Millennium RadNet Auto Launch Study and Auto Launch Report software functionalities. |
| Product code | LLZ |
| Recalling firm | Cerner Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 29, 2007 |
| 510(k) numbers | K022881 |
| FEI number | 1931259 |
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