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U.S. Department of Health and Human Services

Enforcement Report - Week of August 28, 2013

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Product Detail

Product Description Duet DHA 400, 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 44118-807-30) --- Also Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-807-30)
Recall Number D-895-2013
Classification Class III
Code Info NDC 44118-807-30 Lots 40614, exp. 9/14 and 40614A, exp. 9/14 NDC 76331-807-30 lot 39736A, exp. 3/2014, and lot 41667, exp. 12/2014
Product Distributed Qty 1,460 and 2,990
Reason For Recall Subpotent; Beta carotene (Vitamin A)

Event Detail

Event Id 65663
Product Type Drugs
Status Ongoing
Recalling Firm Stayma Consulting Service, LLC.
City Suwanee
State GA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-06-28
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide.