Alpha Woman Original Capsules recalled for undeclared milk
NutraCap Labs LLC is recalling Alpha Woman Original Capsules (60ct Bottle, UPC 11883 60220) because the product contains undeclared milk, a common allergen that poses a risk to consumers with milk allergies.
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 recall is classified as FDA Class I by the agency, which requires a severity score of at least 4. Undeclared milk is a common allergen that poses a serious risk of allergic reaction in susceptible consumers, meeting the threshold for a Severe classification.
Plain-English summary
NutraCap Labs LLC is recalling Alpha Woman Original Capsules, 60ct Bottle (UPC CODE 11883 60220, LOT #2011027, EXP DATE 11/2022) due to the presence of undeclared milk in the product. During an FDA investigation, the firm was notified that the product contains undeclared milk.
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 by this recall.
Consumers who have purchased this product and have a milk allergy or sensitivity should stop using it and consult their healthcare provider if they have consumed it. Consumers should return the product to the place of purchase for a refund or contact NutraCap Labs LLC for further instructions.
The recalled product
- Product
- Alpha Woman Original Capsules, 60ct Bottle, UPC CODE 11883 60220
- 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 (2)
- LOT #2011027
- EXP DATE 11/2022
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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