Recall · openFDA Food Enforcement

Pharmanex Cortitrol. Cortisol Management. 60 Capsules: FDA Recall F-1579-2017

Agency action: Feb 13, 2017Record ID: F-1579-2017
View official source ↗

What happened

Original notice title

Pharmanex Cortitrol. Cortisol Management. 60 Capsules, recall F-1579-2017

From the archived source record

Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Mar 15, 2017
Termination date in the archive
Aug 22, 2017
Source checked
Jul 16, 2026
Record revision
4c6671293df3

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Company
Nu Skin Enterprises Inc.
Lot / identifier
Batches: DL06951-08, DL14251-08, DL34351-08, DL06061-08, DL27161-08
Market / distribution
Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.