Botanical Be recalls Kuka Flex Forte caplets (30-count bottles) due to undeclared diclofenac. All lots produced by Kukamonga in Guadalajara, Mexico, expiring Dec 2024.
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Botanical Be is recalling all Kuka Flex Forte caplets in 30-count bottles because they contain undeclared diclofenac, a painkiller that can cause serious health risks. This affects people who take these caplets for pain relief without knowing the medication contains an unapproved drug.
Diclofenac is a painkiller that requires FDA approval for use in the U.S. The caplets contain this drug without proper approval, which can lead to serious health issues like stomach bleeding or kidney damage if taken without medical supervision.
People who own or use Kuka Flex Forte caplets in 30-count bottles manufactured by Kukamonga in Guadalajara, Mexico, with expiration dates through December 2024. Those taking pain medication without knowing the caplets contain diclofenac are most at risk.
Check for Kuka Flex Forte caplets in 30-count bottles with the manufacturer address: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, Mexico. The product has a UPC code 0736640810265 and expires by December 2024.
Look for the manufacturer address and UPC code on the caplet packaging to confirm it matches the recalled items.
Diclofenac is a painkiller that requires FDA approval for use in the U.S. The caplets contain this drug without proper approval, which can lead to serious health issues like stomach bleeding or kidney damage if taken without medical supervision.
Check for Kuka Flex Forte caplets in 30-count bottles with the manufacturer address: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, Mexico. The product has a UPC code 0736640810265 and expires by December 2024.
The recall record does not specify a remedy, so you should contact the manufacturer directly for guidance.
We’ve drafted a message you can send Botanical Be to request your refund or repair — edit it as you like.
Subject: Recall D-0226-2024 — Botanical Be Botanical Be Hello, I own a Botanical Be that is covered by recall D-0226-2024 from Botanical Be. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
