Kirkland Signature Organic Soy Non-Dairy Beverage Vanilla; 12- 32 oz. cartons (note- 12 count consumer display case) SunOpta Item number 1243803 Individual Carton UPC: 0 96619 99861 6; 12 x 32 oz. container carton UPC: 096619 49000 4 Ambient, keep refrigerated after opening. Best if used within 7 10 days after opening, not to be used as infant formula. Distributed by: Costco Wholesale Corporation P.O. Box 34535 Seattle, WA 98124
Class I - DangerousWhat Should You Do?
- Check if you have this product: 07 DEC 2022 11821341E XX:XX; 08 DEC 2022 11821342E XX:XX
- 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:
- SunOpta Grains and Foods Inc.
- Reason for Recall:
- Product that did not meet quality standards was released in error. Complaints of spoilage received.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Kirkland Signature Organic Soy Non-Dairy Beverage Vanilla; 12- 32 oz. cartons (note- 12 count consumer display case) SunOpta Item number 1243803 Individual Carton UPC: 0 96619 99861 6; 12 x 32 oz. container carton UPC: 096619 49000 4 Ambient, keep refrigerated after opening. Best if used within 7 10 days after opening, not to be used as infant formula. Distributed by: Costco Wholesale Corporation P.O. Box 34535 Seattle, WA 98124
Product Codes/Lot Numbers:
07 DEC 2022 11821341E XX:XX; 08 DEC 2022 11821342E XX:XX
Distribution:
Distributed in: AZ, CA, WA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0631-2022
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