Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton UPC 087684001004. Four cartons per wholesale case.
Class I - DangerousWhat Should You Do?
- Check if you have this product: The Best When Used By date on the products is June 25, 2023 Carton code: 25JUN2023 WXX #### CT1404 Notes: XX may be 01, 02, or 03 #### would be between 0733-1000 Pouch code: 25JUN2023 WXX LYY #### Notes: XX may be 01, 02, 03, 04, 09, or 10. YY may be 01 through 12 #### would be between 0733-0900
- 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:
- KRAFT HEINZ FOODS COMPANY
- Reason for Recall:
- cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton UPC 087684001004. Four cartons per wholesale case.
Product Codes/Lot Numbers:
The Best When Used By date on the products is June 25, 2023 Carton code: 25JUN2023 WXX #### CT1404 Notes: XX may be 01, 02, or 03 #### would be between 0733-1000 Pouch code: 25JUN2023 WXX LYY #### Notes: XX may be 01, 02, 03, 04, 09, or 10. YY may be 01 through 12 #### would be between 0733-0900
Distribution:
Distributed in: IL, IN, MD, MS, NJ, NY, PA, VA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1735-2022
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