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FDAFDA · Food and drugs·Recall number D-894-2013

Duet DHA Balanced, 1) 30 count tablet blister cards and 5 count softgels blister cards combination pack (NDC 44118-775-30 and NDC 44118-800-30) 2) physician samples (carton contain 7 envelopes each with one 5 count tablet blister card and 5 softgels (NDC 44118-800-05) Rx only, Manufactured for Eckson Labs, Wilmington, DE

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
1) NDC 44118-775-30, Lots 12120001, exp. 10/14 and 12120002, exp. 10/14; NDC 44118-800-30, Lots 12120001, exp 10/14 and 12080002, exp 8/14 2) Physician Samples: NDC 44118-800-05, Lot 12080001 exp. 8/14 and 12120002, exp. 10/14
Risk classification
Class III
Area (FDA)
drug
Country
United States

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