Botanical Be: Drug Recall
Recall #D-0226-2024 · 10/20/2023
Class I: Dangerous
Recall Details
- Recall Number
- D-0226-2024
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- Botanical Be
- Status
- Ongoing
- Date Initiated
- 10/20/2023
- Location
- El Paso, TX, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 300 bottles
Reason for Recall
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Product Description
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Distribution Pattern
USA Nationwide
Other Recalls by Botanical Be
- Class I: Dangerous 10/20/2023
- Class I: Dangerous 10/20/2023
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.