MODERATE RISK
Terminated
F-1578-2017
Pharmanex BioGinkgo. Mental Sharpness. 60 Tablets
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 BioGinkgo due to undeclared allergen; wheat.
Product Details
Product Quantity
40,158
Product Type
Food
Code Info
Batches: DL14951-07, DL31551-07, DL21161-07
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
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