Device recall
Z-1827-2008: MIM 4.0 and MIM 4.1 is a software package designed for use in diagnostic…
FDA device recall · Class II · MIMvista Corp
Key facts
| Recall number (Z-number) | Z-1827-2008 |
|---|---|
| Recall event | 48114 |
| Product | MIM 4.0 and MIM 4.1 is a software package designed for use in diagnostic imaging. It is a stand alone software package which operates on Windows 2000/XP. |
| Product code | LLZ |
| Recalling firm | MIMvista Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2015 |
| 510(k) numbers | K060816, K071964 |
| FEI number | 3004363352 |
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