D-895-2013 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
- 1,460 and 2,990
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)
Reason for Recall
Subpotent; Beta carotene (Vitamin A)
Distribution Pattern
Nationwide.
Code Information
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