Status
Terminated
Drug Enforcement D-895-2013
Subpotent; Beta carotene (Vitamin A)
Classification
Class III
Report Date
August 28, 2013
Termination Date
May 27, 2014
Product Information
- 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)
- Product quantity
- 1,460 and 2,990
- Reason for recall
- Subpotent; Beta carotene (Vitamin A)
- Recall initiation reason
- —
- Initial firm notification
- Letter
- Distribution pattern
- Nationwide.
Location & Firm
- Recalling firm
- Stayma Consulting Service, LLC.
- Address
-
5400 Laurel Springs Pkwy, Suite 803
United States - Voluntary / Mandated
- Voluntary: Firm initiated
- Status date
- —
Codes & Dates
- Recall number
- D-895-2013
- Event ID
- 65663
- Recall initiation date
- June 28, 2013
- Center classification date
- August 16, 2013
- Code info
- 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
- More code info
- —