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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Snacks & Confections

THE SAPPHIRE EXCHANGE: Yum Crumbs Strawberry Shortcake Recalled for Undeclared Red #40

Agency Publication Date: March 5, 2021
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Summary

The Sapphire Exchange is recalling approximately 3,421 bottles of Yum Crumbs Strawberry Shortcake in 12 oz and 32 oz sizes. This product contains Red #40, a color additive that was not declared on the ingredient label. Consumers who have purchased these products should return them to the place of purchase for a full refund.

Risk

Red #40 can cause allergic-type reactions in sensitive individuals. While the risk level is categorized as low, individuals with a sensitivity to this color additive may experience adverse reactions if the product is consumed.

What You Should Do

  1. Check your kitchen or pantry for bottles of Yum Crumbs Strawberry Shortcake in 12 oz or 32 oz sizes.
  2. Identify affected products by checking for recall number F-0333-2021.
  3. Immediately stop using the product if you or someone in your household has a sensitivity or allergy to Red #40.
  4. Return any affected product to the place of purchase for a full refund, or contact The Sapphire Exchange for further instructions.
  5. For additional information or questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Full refund upon return.

How to: Return to the place of purchase for a full refund or contact the manufacturer for further instructions.

Affected Products

Product: Yum Crumbs Strawberry Shortcake (12 oz)
Item Code:
F-0333-2021
Product: Yum Crumbs Strawberry Shortcake (32 oz)
Item Code:
F-0333-2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87405
Status: Resolved
Manufacturer: THE SAPPHIRE EXCHANGE
Sold By: Domestic retailers
Manufactured In: United States
Units Affected: 3,421 bottles
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.