Antidepressant recalled over impurity linked to potential cancer risk.
FDA recalled 370k duloxetine bottles for carcinogenic N-nitroso contamination; second Breckenridge recall within 90 days. Supply chain governance signal: repeated manufacturing failures indicate systemic oversight gaps—critical for pharmatech and regulated-product leaders.
More than 370,000 bottles of the common antidepressants have been recalled over the concerns.