The Recall Desk
ModerateFDA (Drugs)·D-898-2013·Announced 2013-08-28

Stayma Recalls Duet DHA 430 Vitamins for Subpotent Beta Carotene

Stayma Consulting Service is recalling Duet DHA 430 vitamin and Omega-3 products because the beta carotene (Vitamin A) content is subpotent.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class III, which indicates a remote possibility of adverse health consequences. The hazard is a subpotent ingredient (beta carotene/Vitamin A), which is a quality issue rather than a high-risk contamination or acute safety hazard.

Plain-English summary

Stayma Consulting Service, LLC. is recalling 2,985 units of Duet DHA 430, a product containing one 30-count bottle of multi-vitamin tablets and one 30-count bottle of Omega-3 softgel capsules. The product is manufactured for W.H. Nutritionals, Wilmington, DE, and carries NDC 76331-808-30.

The recall is due to the product being subpotent, specifically regarding the beta carotene (Vitamin A) content. The affected lots are 39736A (expiration 3/14) and 41667 (expiration 12/14). The products were distributed nationwide.

Consumers who have these products should stop using them and contact the recalling firm for instructions on how to return or dispose of the items.

The recalled product

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
Manufacturer
Stayma Consulting Service, LLC.
Category
Drug — Dietary Supplement
Hazard
Affected units
2,985

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 (4)

  • NDC 76331-808-30
  • lot 39736A
  • exp. 3/14 and lot 41667
  • exp. 12/14

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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Same hazard · subpotent ingredient

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