FDA recall record

keen-wah i heart keenwah Almond All Natural Quinoa Clusters recall — FDA F-1750-2014

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…

Class IIclassification
F-1750-2014official record ID
Apr 16, 2014report date

Recall record at a glance

Official recordF-1750-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmkeen-wah LLC
Report dateApr 16, 2014
Recall initiation dateMar 28, 2014
Quantityapproximately 4899 cs - 4 oz 12 units/case; approximately 475 cs - 1 oz 24 units/cs
LocationChicago, IL, United States

Official product description

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

Why the product 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.

Distribution information

Nationwide and Canada

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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