FDA Class II Recall Issued for Roche's navify Digital Pathology Software
Ventana Medical Systems recalls 190 units of navify Digital Pathology software due to image/metadata discrepancy.
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Ventana Medical Systems recalls 190 units of navify Digital Pathology software due to image/metadata discrepancy.
An FDA enforcement report lists an ongoing nationwide recall of a 60-capsule supplement after agency analysis found unapproved ingredients.