Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Class I - DangerousWhat Should You Do?
- Check if you have this product: All lots, exp 12/12/2024
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Botanical Be
- Reason for Recall:
- Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Product Codes/Lot Numbers:
All lots, exp 12/12/2024
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0226-2024
Related Recalls
Class I - Dangerous
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Class I - Dangerous
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.