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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

Mi More Snacks Coco Bandera Recalled for Undeclared Color

Agency Publication Date: March 13, 2025
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Summary

San Miguel Nuts Corp. is recalling Mi More snacks Coco Bandera sold in 3 oz. plastic containers. Approximately 3,026 bars are affected by this recall because the product label fails to declare a color additive used in the snack. No incidents or injuries have been reported to date.

Risk

The product contains a color additive that is not disclosed on the packaging. This may pose a health risk to consumers with specific sensitivities or allergies to certain food colorings.

What You Should Do

  1. This recall affects Mi More snacks Coco Bandera, which are sold in 3 oz. plastic containers (8 units per container and 20 containers per case box).
  2. Return the product to the place of purchase for a full refund, throw it away, or contact San Miguel Nuts Corp. for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Mi More snacks, Coco Bandera (3 oz.)
Variants: 8 per container, 20 per case box

Recall number F-0629-2025. Approximately 3,026 bars affected.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96254
Status: Resolved
Manufacturer: San Miguel Nuts Corp.
Manufactured In: United States
Units Affected: 3,026 bars.
Distributed To: New Jersey

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 ยท 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.