FDA Drug recall D-899-2013
Duet DHA 430 ec, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsule…
- FDA Drug
- Class III
- terminated
- Published 2013-08-28
On 2013-08-28 the FDA classified a Class III recall of Duet DHA 430 ec, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsule… by Stayma Consulting Service, citing subpotent; Beta carotene (Vitamin A).
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-899-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-06-28 |
| Published | 2013-08-28 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Stayma Consulting Service |
| Distribution | US |
Product
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
Subpotent; Beta carotene (Vitamin A)
Identifiers
| code_info | NDC 76331-810-30; Lot 39736A, exp. 3/14 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-899-2013%22
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