AIOS Synergy for Women Capsules recalled for undeclared milk
NutraCap Labs LLC is recalling AIOS Synergy for Women Capsules (120ct Bottle, Lot 2102130, expiration 02/2023) because the product contains undeclared milk. Consumers with milk allergies or sensitivities who purchased this product should not use it.
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: The FDA classified this as a Class I recall. Per the rubric, FDA Class I recalls are never scored below 4. Undeclared milk is a common allergen that poses immediate risk of serious allergic reaction to sensitive consumers.
Plain-English summary
NutraCap Labs LLC is recalling AIOS Synergy for Women Capsules in 120-count bottles (Lot 2102130, expiration date 02/2023) because the product contains undeclared milk.
During an FDA investigation, the firm was notified that the product contains undeclared milk. This poses a health risk to consumers with milk allergies or sensitivities who may consume the product unknowingly.
The affected 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. A total of 80,169 various bottles and jars are subject to this recall.
Consumers who have purchased this product should stop using it and contact the manufacturer or their healthcare provider if they have consumed it and have concerns about a possible allergic reaction.
The recalled product
- Product
- AIOS Synergy for Women Capsules 120ct Bottle
- 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 2102130 Exp Date 02/2023
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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