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Recall Observatory FDA recall evidence

Drug product

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)

D-896-2013

June 28, 2013

Class III

Product summary

Firm
Stayma Consulting Service, LLC.
Event
Event 65663
Status
Terminated
Classification
Class III
Quantity
NDC 44118-809-30; 747 and NDC 76331-807-30; 1493
Official record key
drug-enforcement:D-896-2013

Official wording

Reason: Subpotent; Beta carotene (Vitamin A)

Code information: NDC 44118-809-30; Lot 40614B, exp. 9/14 and NDC 76331-809-30; lot 39736A, exp. 3/2014,

Distribution pattern: Nationwide.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Subpotent