FDAFDA · Food and drugs·Recall number D-896-2013
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)
Published August 28, 2013 · Recall initiated: June 28, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Subpotent; Beta carotene (Vitamin A)
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stayma Consulting Service, LLC.
- Distributor
- Nationwide.
- Lot
- NDC 44118-809-30; Lot 40614B, exp. 9/14 and NDC 76331-809-30; lot 39736A, exp. 3/2014,
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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