FDAFDA · Food and drugs·Recall number D-0226-2024
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Published December 6, 2023 · Recall initiated: October 20, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Botanical Be
- Distributor
- USA Nationwide
- Lot
- All lots, exp 12/12/2024
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.