Device recall
Z-1267-2025: MIM software; System, Image Processing, Radiological
FDA device recall · Class II · MIM Software Inc
Key facts
| Recall number (Z-number) | Z-1267-2025 |
|---|---|
| Recall event | 96314 |
| Product | MIM software; System, Image Processing, Radiological |
| Product code | LLZ |
| Recalling firm | MIM Software Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | 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