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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/Packaged & Processed

Calais Brand Grape Jelly Recalled for Undeclared Food Colors

Agency Publication Date: July 7, 2025
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Summary

Elwood International, Inc. has voluntarily recalled 43 cases of Calais Brand Grape Jelly sold in 1 gallon (128 FL. OZ.) containers because the product contains the food colors FD&C Blue 1 and FD&C Red 40, which are not declared on the ingredient label. The jelly was distributed to locations in New York and New Jersey. No incidents or injuries have been reported in connection with this recall.

Risk

Consumers who have a severe sensitivity or allergy to FD&C Blue 1 or FD&C Red 40 may experience an adverse reaction if they consume this product.

What You Should Do

  1. The recalled product is Calais Brand Grape Jelly sold in 1 gallon (128 FL. OZ. / 3.785 L) plastic containers with UPC 040264101280 and product order number W-101-28.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact the manufacturer 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 questions.

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: Calais Brand Grape Jelly (128 FL. OZ. / 1 GAL.)
Variants: 128 FL. OZ. (1 GAL.) 3.785 L
Item Code:
W-101-28
UPC Codes:
040264101280

Ingredients listed: Grape Juice, Corn Syrup, High Fructose Corn Syrup, Pectin, Citric Acid; Refrigerate after opening.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97124
Status: Resolved
Manufacturer: Elwood International, Inc.
Manufactured In: United States
Units Affected: 43 cases
Distributed To: New York, New Jersey
Agency Last Updated: July 10, 2025

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.