Reported Dec 6, 2023 · Ongoing
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro,…
Botanical Be
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Botanical Be · 360 Jardin Bello · El Paso, TX · 79932-2357
Is this the product you have?
- Kuka Flex Forte caplets, packaged in 30-count bottles
- Manufactured by
KukamongaGonzalez Ortega No 170 Col Centro44100 Guadalajara JalUPC 0736640810265
- Lot codes and dates
- All lots, exp 12/12/2024
- Amount recalled
- 300 bottles
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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