Severity
Moderate
FDA Food recall · Reported March 15, 2017
Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
Nu Skin Enterprises Inc. recalled Pharmanex Cortitrol. Cortisol Management. 60 Capsules - a moderate-severity action.
Pharmanex Cortitrol. Cortisol Management. 60 Capsules was recalled by Nu Skin Enterprises Inc. in March 15, 2017. Reason: Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.. Check the official notice for the remedy. Verify recall #F-1579-2017 with the FDA Food before acting.
The recall
Nu Skin Enterprises Inc. issued this moderate-severity FDA Food recall-Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy..
Sourced from official FDA Food enforcement records. Verify recall #F-1579-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1579-2017) was formally reported on March 15, 2017, with the manufacturer initiating the action on February 13, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Nu Skin Enterprises Inc. is listed as the recalling firm, operating out of Provo, UT. Federal records list the affected scope as 56,332.
The documented reason for this recall is: Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy. Distribution data in the federal record shows the product reached: Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
56,332
Related Recalls
6
2 from same agency
Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1579-2017 |
| Date reported | March 15, 2017 |
| Date initiated | February 13, 2017 |
| Recalling firm | Nu Skin Enterprises Inc. |
| Firm location | Provo, UT |
| Affected scope | 56,332 |
| Distribution | Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported March 15, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.