Hermes Medical recalls Hybrid Recon software versions 4.0.0x and 5.0.0 for potential incorrect SPECT/CT study alignment. Affected units include Hermes Medical Imaging Suite v6.1 with specific UDI codes and serial numbers.
Due a potential software/configuration issue that may result is incorrect alignment during reconstructing a SPECT/CT study.
Hermes Medical is recalling Hybrid Recon software versions 4.0.0x and 5.0.0 for the potential of incorrect SPECT/CT study alignment. This could affect medical imaging accuracy in certain scans.
The software may misalign SPECT/CT studies during reconstruction, leading to inaccurate medical imaging. This could affect diagnosis and treatment decisions for patients.
Healthcare providers using Hermes Medical Imaging Suite version 6.1 with the affected software versions are most at risk. Patients undergoing SPECT/CT scans may be impacted by inaccurate imaging results.
Check if your Hermes Medical Imaging Suite is version 6.1 with Hybrid Recon software versions 4.0.0x or 5.0.0. UDI-DI codes and serial numbers are listed in the recall notice.
Verify your Hybrid Recon software version on Hermes Medical Imaging Suite version 6.1.
The recall addresses a potential issue with SPECT/CT study alignment, but it does not indicate a risk of serious injury or death. The hazard level is low risk.
Hybrid Recon software versions 4.0.0x and 5.0.0 are affected.
Check your Hermes Medical Imaging Suite version 6.1 and Hybrid Recon software version. Affected units have specific UDI-DI codes and serial numbers listed in the recall notice.
We’ve drafted a message you can send Hermes Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0678-2025 — Hermes Medical Hermes Medical Hello, I own a Hermes Medical that is covered by recall Z-0678-2025 from Hermes Medical. 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.
