BAPS Shayona is recalling coconut fudge products containing undeclared soy due to FDA inspection findings. Consumers should check for the UPC 53119 label and contact the company for details.
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
BAPS Shayona is recalling coconut fudge products that contain undeclared soy, which was discovered during an FDA inspection. This recall affects products sold with the UPC 53119 label. The issue poses a risk for people with soy allergies who may react to the hidden soy ingredient.
The hazard occurs because some BAPS Shayona coconut fudge products contain soy that was not listed on the label. This can cause allergic reactions in individuals sensitive to soy, particularly those with severe allergies who may experience symptoms like swelling, hives, or difficulty breathing.
People who have soy allergies are at risk of adverse reactions from consuming products with undeclared soy. The recall applies to specific coconut fudge items sold in the United States with the UPC 53119 label.
Check for the UPC 53119 label on the product packaging. The product is a 12-ounce coconut fudge sold by BAPS Shayona in Lilburn, GA. The best by date is July 19, 2023.
Look for the UPC 53119 label on the coconut fudge packaging to confirm if it is part of the recall.
The FDA notified BAPS Shayona that some products contain undeclared soy, which can cause allergic reactions in sensitive individuals.
Check the product label for the UPC 53119. If you have the product, contact BAPS Shayona for further instructions.
No, the product contains undeclared soy, which can cause allergic reactions in people with soy allergies.
We’ve drafted a message you can send BAPS Shayona to request your refund or repair — edit it as you like.
Subject: Recall F-0492-2024 — BAPS Shayona BAPS Shayona Hello, I own a BAPS Shayona that is covered by recall F-0492-2024 from BAPS Shayona. 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.
