Milk and Dark Chocolate Caramels Recalled for Undeclared Soy Lecithin
R & S Roberts Enterprises recalls Milk & Dark Chocolate Caramel Macchiato candies distributed in Washington due to undeclared soy lecithin. Consumers with soy allergies should not consume the product.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This recall involves allergen mislabeling (soy lecithin) on a common allergen, which constitutes a score 3 (High) per the FDA severity rubric. No illnesses or injuries have been reported.
Plain-English summary
R & S Roberts Enterprises, Inc. is recalling Milk & Dark Chocolate Caramel Macchiato candies due to undeclared soy lecithin. The product consists of chocolate-coated caramels packaged in 48-piece units and distributed in Washington.
The product labels do not declare soy lecithin, which is present in the finished product. Soy is a common allergen that can trigger allergic reactions in sensitive individuals.
The affected product has a manufacture date of 03/22/2022 (UPC 7 82565 11777 4). Consumers who have purchased this product should stop consuming it immediately and discard any remaining units. Anyone who has consumed the product and experiences allergic symptoms should seek medical attention.
The recalled product
- Product
- Milk & Dark Chocolate Caramel Macchiato. Chocolate coated caramels packaged in bulk and distributed in bulk to the firm's stores in a bin. UPC 7 82565 11777 4.
- Manufacturer
- R & S Roberts Enterprises, Inc.
- Category
- Food — Chocolate / Confectionery
- Affected units
- 48
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Manufacture date: 03/22/2022 Tracking By Manufacture Date: 03/22/2022
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 6 recalled by R & S Roberts Enterprises, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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