D-896-2013 Class III Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- August 28, 2013
- Initiation Date
- June 28, 2013
- Termination Date
- May 27, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- NDC 44118-809-30; 747 and NDC 76331-807-30; 1493
Product Description
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)
Reason for Recall
Subpotent; Beta carotene (Vitamin A)
Distribution Pattern
Nationwide.
Code Information
NDC 44118-809-30; Lot 40614B, exp. 9/14 and NDC 76331-809-30; lot 39736A, exp. 3/2014,