i heart keenwah recalls ginger peanut quinoa clusters with soy lecithin not declared on labels. Check UPCs 736211802644 (4oz) and 713757598408 (1oz).
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.
i heart keenwah is recalling ginger peanut quinoa clusters because soy lecithin was used in production but not listed on labels. This could mislead consumers about ingredients, though it doesn't pose a direct health risk.
Soy lecithin was added as an anti-stick spray during manufacturing but wasn't declared on product labels. This means consumers might not know if they have soy lecithin in their food, which could be a concern for those with soy allergies.
Owners of i heart keenwah ginger peanut quinoa clusters with UPC 736211802644 (4oz) or 713757598408 (1oz) are affected. People with allergies to soy lecithin may be at slightly higher risk.
Check for UPC 736211802644 (4oz) or 713757598408 (1oz) on the product packaging. The product codes all read EXPDDMMYY (expiration date format).
Look for the UPC codes 736211802644 (4oz) or 713757598408 (1oz) on the packaging.
The recall is due to soy lecithin not being listed on labels, not a safety hazard. It is safe to eat but consumers should check labels for soy allergies.
Check the UPC codes on your packaging. If it matches the recalled codes, you may want to contact i heart keenwah for more information.
No, the recall is about labeling, not a physical hazard. There is no risk of injury from this product.
We’ve drafted a message you can send i heart keenwah to request your refund or repair — edit it as you like.
Subject: Recall F-1751-2014 — i heart keenwah i heart keenwah Hello, I own a i heart keenwah that is covered by recall F-1751-2014 from i heart keenwah. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.