Class I Recall

Botanical Be

Product
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Reason
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Classification
Class I
Status
Ongoing
Lot
All lots, exp 12/12/2024
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.