Liquid Lucky Kiwi Lime Sample Recalled for Undeclared Milk
NutraCap Labs LLC is recalling Liquid Luck Liquid Lucky Kiwi Lime Sample bottles and jars because they contain undeclared milk, a major allergen. The product was distributed across 25 US states.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: This is an FDA Class I recall involving undeclared milk, a major allergen. Allergen mislabeling on common allergens with the potential to cause serious harm in sensitive populations meets the Severe criteria, particularly at this classification level.
Plain-English summary
NutraCap Labs LLC is recalling Liquid Luck Liquid Lucky Kiwi Lime Sample products due to the presence of undeclared milk. During an FDA investigation, the firm was notified that the product contains undeclared milk, which is not declared on the label.
Approximately 80,169 various bottles and jars were affected. The recalled lot is LOT # 2002006/651 with expiration date 02/2022. The product was shipped 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.
Milk is a major allergen and can cause serious allergic reactions in people with milk allergies or lactose intolerance. Consumers who have purchased this product and have a milk allergy or sensitivity should not consume it and should contact their healthcare provider if they have experienced any adverse reactions.
The recalled product
- Product
- Liquid Luck Liquid Lucky Kiwi Lime Sample NO UPC CODE
- Manufacturer
- NutraCap Labs LLC
- Category
- Food — Beverage / Drink Mix
- 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 # 2002006/651 EXP DATE 02/2022
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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