Botanical Be recalls Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44
Recalled December 6, 2023 · FDA recall D-0226-2024 · Botanical Be
Hazard
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac. · FDA Class I
Units
300 bottles
Sold at
USA Nationwide
Description
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Product
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Manufacturer(s)
Botanical Be
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →