MODERATE RISK
Terminated
F-1579-2017
Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Recalled by Nu Skin Enterprises Inc.
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
Reason for Recall
Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
Product Details
Product Quantity
56,332
Product Type
Food
Code Info
Batches: DL06951-08, DL14251-08, DL34351-08, DL06061-08, DL27161-08
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.
Company Location
Provo, UT, 84601-4432
Timeline
Report Date
03/15/2017
Recall Initiated
02/13/2017
Classification Date
03/08/2017
Termination Date
08/22/2017
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: July 13, 2026
Related Recalls
Get Real-Time Recall Alerts on Your Phone
Scan any grocery receipt and instantly know if your food has been recalled. Free download — protect your family in 3 seconds.
