FDAOctober 20, 2023drug

Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

What to do

FDA enforcement status: Ongoing

Brands named

botanical bebotanical

UPCs

0736640810265

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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