According to the December 6, 2023, FDA Enforcement Report, the recall affects all Kuka Flex Forte caplets (UPC 0736640810265), which are packaged in 100-count bottles. The caplets were manufactured by Kukamonga, Guadalajara, Jalisco, Mexico,...
According to the December 6, 2023, FDA Enforcement Report, the recall affects all Kuka Flex Forte caplets (UPC 0736640810265), which are packaged in 100-count bottles. The caplets were manufactured by Kukamonga, Guadalajara, Jalisco, Mexico,...
According to the December 6,...