Duet DHA 430 ec Recalled for Subpotent Beta Carotene
Stayma Consulting Service is recalling Duet DHA 430 ec because the beta carotene (Vitamin A) content is subpotent.
The agency’s classification
FDA (Drugs): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
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 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which indicates the product is not likely to cause adverse health consequences. The hazard is a subpotent ingredient, which is a minor labeling or quality issue.
Plain-English summary
Stayma Consulting Service, LLC. is recalling 1,492 units of Duet DHA 430 ec, a combination of multi-vitamin tablets and Omega-3 softgel capsules. The product was manufactured for W.H. Nutritionals, Wilmington, DE, and is identified by NDC 76331-810-30, Lot 39736A, with an expiration date of 3/14.
The recall was initiated because the product contains subpotent levels of beta carotene (Vitamin A). This means the amount of the active ingredient is less than the labeled amount.
The product was distributed nationwide. Consumers who have this product should stop using it and contact the recalling firm for instructions on how to return it or obtain a refund.
The recalled product
- Product
- Duet DHA 430 ec, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-810-30)
- Manufacturer
- Stayma Consulting Service, LLC.
- Category
- Drug — Dietary Supplement
- Hazard
- Affected units
- 1,492
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 (3)
- NDC 76331-810-30
- Lot 39736A
- exp. 3/14
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 7 recalled by Stayma Consulting Service, LLC. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 7 products in this recall →Related recalls
Same manufacturer · Stayma Consulting Service, LLC.
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FDA (Drugs) · 2013-08-28
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