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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

Fila Manila Coconut Jam Recalled for Undeclared Gluten

Agency Publication Date: October 4, 2022
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Summary

Fila Manila Corporation is recalling 1,340 units of Fila Manila Coconut Jam (12 oz) because it contains gluten that was not listed on the product label. The recall was initiated after gluten was found in the jam, which could affect consumers who need to avoid gluten for health reasons. No illnesses or injuries have been reported to date regarding this product.

Risk

People who have an allergy or severe sensitivity to gluten, or those with celiac disease, may experience an adverse health reaction if they consume this product.

What You Should Do

  1. This recall affects 12 oz jars of Fila Manila Coconut Jam with UPC 860003619353, lot number 6196, and a Best By date of 6/30/24.
  2. Return the product to the place of purchase for a refund, throw it away, or contact Fila Manila Corporation for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) 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: Fila Manila Coconut Jam (12 oz / 340g)
UPC Codes:
860003619353
Lot Numbers:
6196 (Exp 6/30/24)

Recall number F-0004-2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90893
Status: Resolved
Manufacturer: Fila Manila Corporation
Sold By: distributors
Manufactured In: United States
Units Affected: 1,340 units
Distributed To: Indiana, Nevada

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.