D-894-2013 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) 12,278 and 28476; 2) 23740
Product Description
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
Reason for Recall
Subpotent; Beta carotene (Vitamin A)
Distribution Pattern
Nationwide.
Code Information
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