Duet DHA 400 — Class III drug recall D-895-2013
Terminated recall by Stayma Consulting Service, LLC., reported 2013-08-28, distributed nationwide. Subpotent; Beta carotene (Vitamin A)
| Recall number | D-895-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stayma Consulting Service, LLC., Suwanee, GA, United States |
| Recall initiated | 2013-06-28 |
| Classified | 2013-08-16 |
| Reported by FDA | 2013-08-28 |
| Terminated | 2014-05-27 |
| Distributed | Nationwide (US) |
| Reason classes | potency |
| NDC | 44118-0807-30, 76331-0807-30 |
| Lot numbers | 39736A, 40614, 40614A, 41667, 9/14 |
| Expiration dates | 2014-03, 2014-12 |
Product
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)
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-895-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.