Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta carotene (Vitamin A)
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stayma Consulting Service, LLC. directly.
Affected Products
Duet DHA 400 ec, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Rx only, Manufactured for Eckson Labs, Wilmington, DE (NDC 44118-809-30) and Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-809-30)
Quantity: NDC 44118-809-30; 747 and NDC 76331-807-30; 1493
Why Was This Recalled?
Subpotent; Beta carotene (Vitamin A)
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stayma Consulting Service, LLC.
Stayma Consulting Service, LLC. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report