KABANA SKIN CARE

FDA Initiates Class II Recall of KABANA SKIN CARE's GreenScreen Zinc Oxide Sunscreen Over cGMP Violations

KABANA SKIN CARE has initiated a Class II recall for 174 tubes of its GreenScreen Zinc Oxide Sunscreen (NDC: 73369-0001-1) from its Louisville, CO facility, citing cGMP deviations. This voluntary action, affecting lots 405-002 and 405-003 distributed across NJ, FL, and MI, underscores critical quality control lapses. Procurement and regulatory teams must scrutinize supplier cGMP compliance to mitigate supply chain risks and ensure product integrity for consumer safety.