Drug recall
MIM software; System, Image Processing, Radiological
FDA recall event 96314 · Class II · MIM Software Inc
Key facts
| Event ID | 96314 |
|---|---|
| Recall numbers | Z-1267-2025 |
| Recalling firm | MIM Software Inc |
| Product type | Devices |
| Products | MIM software; System, Image Processing, Radiological |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | In situations where two images with differing Fields of View (FOV) complete an image fusion, an incorrect, elevated Maximum Standardized Uptake Value (SUV) within MIM Software versions 7.2.0 through… |
| Initiation date | Feb 19, 2025 |
| Report date | Mar 12, 2025 |
| City | Cleveland |
| State | OH |
| Country | United States |
| FEI number | 3004363352 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: