R & S Roberts recalls bulk Milk & Dark Chocolate Caramel Macchiato due to undeclared soy lecithin in products. Check UPC 7 82565 11777 4 for affected items manufactured March 22, 2022.
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
R & S Roberts is recalling bulk Milk & Dark Chocolate Caramel Macchiato products because they contain undeclared soy lecithin. This means some consumers may have been exposed to soy lecithin without knowing it, which could pose health risks for certain individuals.
The products were made with canola oil spray as a releasing agent but do not list soy lecithin on their labels. Soy lecithin is a common allergen that can cause allergic reactions in sensitive individuals, including skin rashes, swelling, or breathing difficulties.
People who purchased or consumed the bulk Milk & Dark Chocolate Caramel Macchiato products with UPC 7 82565 11777 4 from R & S Roberts stores. Those with soy allergies or sensitivities are at higher risk.
Check for the UPC 7 82565 11777 4 on the product packaging. The products were manufactured on March 22, 2022, and distributed in bulk to R & S Roberts stores.
Look for the UPC 7 82565 11777 4 on the product packaging to confirm if it's affected.
The recall does not state that the product is unsafe; it indicates that soy lecithin was not declared on the label, which may pose risks for those with soy allergies.
The recall record does not specify a remedy, so there is no action required beyond checking the product label for the UPC 7 82565 11777 4.
The products were manufactured on March 22, 2022.
We’ve drafted a message you can send R & S Roberts to request your refund or repair — edit it as you like.
Subject: Recall F-1064-2022 — R & S Roberts R & S Roberts Hello, I own a R & S Roberts that is covered by recall F-1064-2022 from R & S Roberts. 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.
