Finax Muesli Recall: Undeclared Coconut Allergen Risk
Chicago Importing Co recalls Finax Muesli (22.9 oz) because the label does not list coconut, posing a risk to those with allergies.
Use caution until it’s fixed
The product's ingredients statement does not indicate presence of coconut
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What happened, in plain English
Chicago Importing Co is recalling Finax Muesli with 45% Fruit because the ingredient statement fails to indicate the presence of coconut. This omission poses a health risk to consumers with coconut allergies who rely on the label for safety information. The recall affects approximately 2,700 retail bags distributed across several states. Read more at govinfonow.com/recall/18075-finax-muesli-recall-undeclared-coconut-allergen-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/18075-finax-muesli-recall-undeclared-coconut-allergen-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0672-2019
Cite this page
“Finax Muesli Recall: Undeclared Coconut Allergen Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18075-finax-muesli-recall-undeclared-coconut-allergen-risk. Based on FDA recall #F-0672-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0672-2019%22&limit=1).
Why it’s dangerous
The product contains coconut, but the packaging does not list it as an ingredient. For individuals with a coconut allergy, consuming this product can trigger an allergic reaction because they may unknowingly ingest the allergen.
Who’s affected
Consumers who purchased and possess the specific recalled lots of Finax Muesli are affected. Individuals with coconut allergies or sensitivities are at the highest risk due to the undeclared allergen.
How to tell if you have this one
Check for Finax Muesli with 45% Fruit in a 22.9-oz heat-sealed plastic bag. Verify the CIC Product Number is 91056, Lot code is 1180306, Best By Date is 03/06/2019, and UPC is 7311142201358.
- Brand
Finax- Product
Finax Muesli with 45% Fruit; 22.9-oz.; Heat sealed plastic bag; 10 bags/case- Category
Food
Where it went and when
Where it was distributed
Distributed in 12 states.
FDA distribution: “AZ CA FL IL MA MD MI MN NJ NY VA WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Florida, Illinois, Maryland, Massachusetts, Michigan, Minnesota, New Jersey, New York, Virginia, Washington.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0672-2019 (November 9, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0672-2019 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.