D-899-2013 Class III Terminated
FDA drug recall D-899-2013 was initiated by Stayma Consulting Service, LLC. on June 28, 2013 and is designated Class III. Reason for recall: Subpotent; Beta carotene (Vitamin A) The recall status is terminated (terminated May 27, 2014). Affected quantity: 1492.
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
- 1492
Product Description
Duet DHA 430 ec, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-810-30)
Reason for Recall
Subpotent; Beta carotene (Vitamin A)
Distribution Pattern
Nationwide.
Code Information
NDC 76331-810-30; Lot 39736A, exp. 3/14