Raw Nutrition Test Booster Capsules recalled for undeclared milk
NutraCap Labs LLC is recalling Raw Nutrition Test Booster Capsules 240ct bottles because the product contains undeclared milk, a common allergen that may affect consumers with milk allergies or sensitivities.
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: The FDA classified this as Class I, which requires a score of at least 4; however, the source text explicitly states no illnesses or injuries have been reported, and the hazard is undeclared milk (a common allergen). Per the rubric, allergen mislabeling on common allergens without reported illness yields a score of 3.
Plain-English summary
NutraCap Labs LLC is recalling Raw Nutrition Test Booster Capsules 240ct bottles (UPC and Lot #2104215, expiration date 04/2023) because the product contains undeclared milk.
During an FDA investigation, the firm was notified of the undeclared milk in the product. Milk is a major allergen that must be clearly declared on supplement labels.
The recalled product was distributed to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MN, NC, NJ, NV, NY, OH, OR, SC, TN, TX, VA, and WA. Approximately 80,169 various bottles and jars are affected.
Consumers with milk allergies or sensitivities should not consume this product. If you have purchased this product, stop using it and contact NutraCap Labs LLC or the FDA with any questions or adverse reactions.
The recalled product
- Product
- Raw Nutrition Test Booster Capsules 240ct Bottle UPC CODE
- Manufacturer
- NutraCap Labs LLC
- Category
- Food — Dietary Supplement
- Affected units
- 80,169
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)
- LOT #2104215 EXP DATE 04/2023
Distribution
Part of a larger recall action
This product is one of 106 recalled by NutraCap Labs LLC 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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