Nu Skin Recalls Pharmanex Cholestin Softgels Due to Undeclared Soy Allergen
Nu Skin Enterprises is voluntarily recalling Pharmanex Cholestin softgels because the product contains undeclared soy, a common allergen.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves allergen mislabeling on a common allergen (soy), which corresponds to a severity score of 3 (High) according to the rubric.
Plain-English summary
Nu Skin Enterprises Inc. is conducting a voluntary field action for Pharmanex Cholestin. Cholesterol Health. 60 Softgels. The recall is being issued because the product contains an undeclared allergen: soy.
The affected product is identified by Batch CS10351. A total of 7,327 units were distributed nationwide, to Canadian consignees, and to other foreign consignees. The source text notes that no VA, government, or military consignees were involved.
Consumers with a soy allergy or sensitivity should avoid using this product. Individuals who have already consumed the product and are experiencing symptoms should consult a healthcare professional. Consumers can contact Nu Skin Enterprises for further information regarding the recall.
The recalled product
- Product
- Pharmanex Cholestin. Cholesterol Health. 60 Softgels.
- Manufacturer
- Nu Skin Enterprises Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 7,327
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Batch: CS10351
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by Nu Skin Enterprises Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
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