Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MIM software Recalled by MIM Software Inc Due to In situations where two images with differing Fields...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MIM Software Inc directly.
Affected Products
MIM software; System, Image Processing, Radiological
Quantity: 352 units
Why Was This Recalled?
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 7.2.6.could result.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MIM Software Inc
MIM Software Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report