HERMES MEDICAL SOLUTIONS AB
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (1)
- HERMES MEDICAL SOLUTIONS, AB FEI 3002831423 · SE
Recalls & enforcement
- Class IIOngoing2024-10-31Due a potential software/configuration issue that may result is incorrect alignment during reconstructing a SPECT/CT study.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “HERMES MEDICAL SOLUTIONS AB — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9047204-hermes-medical-solutions-ab/
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