Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Recalling firm: Nu Skin Enterprises Inc.
Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 22, 2017.
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FDA code information
Batches: DL06951-08, DL14251-08, DL34351-08, DL06061-08, DL27161-08
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Full FDA record and distribution details
Original product description
Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Original FDA recall reason
Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
Recall details
- Recall number
- F-1579-2017
- Event ID
- 76535
- FDA status
- Terminated
- Initiated
- Feb 13, 2017
- Reported
- Mar 15, 2017
- Classified
- Mar 8, 2017
- Terminated
- Aug 22, 2017
- Quantity
- 56,332
- Location
- Provo, UT, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.
Data updated September 16, 2026. View official FDA data ↗
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