AIOS Synergy for Women Capsules 120ct Bottle — Class I food recall F-0406-2022
Terminated recall by NutraCap Labs LLC, reported 2022-01-19, distributed in AL, AR, AZ, CA, CO, CT, FL, GA…. During an FDA investigation the firm was notified that the product contains undeclared milk.
| Recall number | F-0406-2022 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | NutraCap Labs LLC, Norcross, GA, United States |
| Recall initiated | 2021-11-09 |
| Classified | 2022-01-11 |
| Reported by FDA | 2022-01-19 |
| Terminated | 2024-05-21 |
| Distributed | 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, WA |
| Quantity | 80,169 various |
| Reason classes | undeclared allergen |
| Allergens | milk |
| Lot numbers | 2102130 |
| Expiration dates | 2023-02 |
Product
AIOS Synergy for Women Capsules 120ct Bottle
Reason for recall
During an FDA investigation the firm was notified that the product contains undeclared milk.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0406-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.