MIM Software versions 7.2.0 through 7.2.6c have a potential issue with image fusion that could result in incorrect Maximum Standardized Uptake Value (SUV) calculations. Affected users should check their software version and contact MIM for details.
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.
MIM Software versions 7.2.0 through 7.2.6c may produce incorrect SUV values during image fusion when images have different fields of view. This could lead to inaccurate medical imaging results if used in radiological applications.
When two images with different fields of view are fused in MIM Software versions 7.2.0 through 7.2.6c, the software may calculate an incorrect, elevated Maximum Standardized Uptake Value (SUV). This could lead to inaccurate medical imaging results if used in radiological applications.
Users of MIM Software versions 7.2.0 through 7.2.6c for radiological image processing are affected. Medical professionals using these versions for medical imaging are most at risk.
Check if you have MIM Software versions 7.2.0 through 7.2.6c, which include specific UDI/DI numbers listed in the recall notice. The affected versions are used for radiological image processing.
Verify your MIM Software version by checking the version number in the software settings or documentation.
MIM Software versions 7.2.0 through 7.2.6c are affected, including specific UDI/DI numbers listed in the recall notice.
The issue could result in incorrect Maximum Standardized Uptake Value (SUV) calculations during image fusion when images have different fields of view, potentially leading to inaccurate medical imaging results.
Check your software version and contact MIM Software directly for further instructions on potential remedies.
We’ve drafted a message you can send MIM Software to request your refund or repair — edit it as you like.
Subject: Recall Z-1267-2025 — MIM Software MIM Software Hello, I own a MIM Software that is covered by recall Z-1267-2025 from MIM Software. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
