i heart keenwah recalls cranberry cashew quinoa clusters due to soy lecithin not being declared on labels. Check UPCs 736211802545 (4oz) and 713757598309 (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 cranberry cashew quinoa clusters because soy lecithin used in production wasn't listed on labels. This could mislead consumers about ingredients, though no safety risks are mentioned in the recall.
The product was made using an anti-stick spray with soy lecithin, but this ingredient wasn't declared on the label. This means consumers might not know they're consuming soy lecithin, which could be important for some dietary needs.
Owners of cranberry cashew quinoa clusters with UPCs 736211802545 (4oz) or 713757598309 (1oz) are affected. People with dietary restrictions requiring full ingredient transparency may be at higher risk.
Check for UPC 736211802545 (4oz) or 713757598309 (1oz) on the product packaging. The product codes all read EXPDDMMYY (expiration dates).
Look for UPC 736211802545 (4oz) or 713757598309 (1oz) on the packaging.
The recall is about ingredient labeling, not safety. The product is safe to eat but may not list soy lecithin as an ingredient.
The manufacturer used an anti-stick spray containing soy lecithin but didn't declare it on the label.
The recall doesn't require action. Check the UPCs to confirm if you have the affected products.
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-1752-2014 — i heart keenwah i heart keenwah Hello, I own a i heart keenwah that is covered by recall F-1752-2014 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.
