Duet DHA 430 Multivitamin (Stayma Consulting) – Subpotent Vitamin A (2013)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Duet DHA 430, 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 76331-808-30
Brand
Stayma Consulting Service, LLC.
Lot Codes / Batch Numbers
NDC 76331-808-30, lot 39736A, exp. 3/14 and lot 41667, exp. 12/14
Products Sold
NDC 76331-808-30; lot 39736A, exp. 3/14 and lot 41667, exp. 12/14
Stayma Consulting Service, LLC. is recalling Duet DHA 430, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-cou due to Subpotent; Beta carotene (Vitamin A). This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Subpotent; Beta carotene (Vitamin A)
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 7, 2026