keen-wah i heart keenwah Almond All Natural Quinoa Recall

Why it was recalled

An anti-stick spray containing soy lecithin was used during the manufacture of several varieties of i heart keenwah, quinoa clusters and soy was not declared on the product labeling.

Product description

i heart keenwah Almond All Natural Quinoa Clusters. UPC 736211802347 for the 4 oz UPC 713757598200 for the 1 oz

Lot numbers, UPCs & expiration codes

All codes which read EXPDDMMYY (all dates)

Where it was sold

Nationwide and Canada

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-1750-2014
Classification: Class II
Status: Terminated
Recall initiated: Mar 28, 2014
FDA report date: Apr 16, 2014
Quantity: approximately 4899 cs - 4 oz 12 units/case; approximately 475 cs - 1 oz 24 units/cs
Recall type: Voluntary: Firm initiated
Recalling firm: keen-wah LLC

Original FDA data

Every field from FDA enforcement report F-1750-2014, exactly as published.

Show all FDA fields

City: Chicago
State: IL
Status: Terminated
Country: United States
Event ID: 67848
Address: 4743 N Hermitage
Code information: All codes which read EXPDDMMYY (all dates)
Postal code: 60640
Report date: Apr 16, 2014
Product type: Food
Recall number: F-1750-2014
Classification: Class II
Recalling firm: keen-wah LLC
Product quantity: approximately 4899 cs - 4 oz 12 units/case; approximately 475 cs - 1 oz 24 units/cs
Termination date: May 13, 2014
Reason for recall: An anti-stick spray containing soy lecithin was used during the manufacture of several varieties of i heart keenwah, quinoa clusters and soy was not declared on the product labeling.
Voluntary / mandated: Voluntary: Firm initiated
Product description: i heart keenwah Almond All Natural Quinoa Clusters. UPC 736211802347 for the 4 oz UPC 713757598200 for the 1 oz
Distribution pattern: Nationwide and Canada
Recall initiation date: Mar 28, 2014
Initial firm notification: Telephone
Center classification date: Apr 4, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1750-2014, published Apr 16, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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