Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Recalled by Hermes Medical Solutions AB Due to Due a potential software/configuration issue that may result...
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 Hermes Medical Solutions AB directly.
Affected Products
Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Hybrid Recon software versions affected are 4.0.0x and 5.0.0
Quantity: 778 systems
Why Was This Recalled?
Due a potential software/configuration issue that may result is incorrect alignment during reconstructing a SPECT/CT study.
Where Was This Sold?
This product was distributed to 15 states: CA, CT, FL, HI, KY, MD, MA, MO, NJ, NY, OH, TN, TX, VA, WA
About Hermes Medical Solutions AB
Hermes Medical Solutions AB 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