BAPS Shayona is recalling sweetened ricotta fudge due to undeclared soy in some products. This recall follows an FDA inspection finding. Consumers should check for the UPC 53037 and best by dates listed.
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
BAPS Shayona is recalling sweetened ricotta fudge products that contain undeclared soy. This recall was initiated after an FDA inspection found some products had soy without being listed on the label. The issue poses a risk for people with soy allergies.
The hazard is that some BAPS Shayona sweetened ricotta fudge products contain soy without being declared on the label. This can cause allergic reactions in people who are sensitive to soy. The risk is specific to individuals with soy allergies.
People with soy allergies are most at risk from this recall. The affected products are sweetened ricotta fudge sold in the United States with the UPC 53037.
Check for the UPC 53037 on the product label. The products were sold with best by dates from July 3, 2023, to July 20, 2023. The products contain milk and are labeled as sweetened ricotta fudge.
Look for the UPC 53037 and best by dates from July 3, 2023, to July 20, 2023.
The FDA found that some BAPS Shayona sweetened ricotta fudge products contain undeclared soy.
Check the product label for the UPC 53037 and best by dates from July 3, 2023, to July 20, 2023. If you have the product, you should avoid it due to the risk of allergic reactions for people with soy allergies.
The recall record does not specify a remedy, so no action is required beyond checking the product label.
We’ve drafted a message you can send BAPS Shayona to request your refund or repair — edit it as you like.
Subject: Recall F-0496-2024 — BAPS Shayona BAPS Shayona Hello, I own a BAPS Shayona that is covered by recall F-0496-2024 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.
