Pharmanex Cortitrol — Class II food recall F-1579-2017
Terminated recall by Nu Skin Enterprises Inc., reported 2017-03-15, distributed nationwide. Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
| Recall number | F-1579-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nu Skin Enterprises Inc., Provo, UT, United States |
| Recall initiated | 2017-02-13 |
| Classified | 2017-03-08 |
| Reported by FDA | 2017-03-15 |
| Terminated | 2017-08-22 |
| Distributed | Nationwide (US) |
| Quantity | 56,332 |
| Reason classes | undeclared allergen |
| Allergens | soy |
| Lot numbers | DL06061-08, DL06951-08, DL14251-08, DL27161-08, DL34351-08 |
Product
Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Reason for recall
Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
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-1579-2017. 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.