Duet DHA Balanced — Class III drug recall D-894-2013
Terminated recall by Stayma Consulting Service, LLC., reported 2013-08-28, distributed nationwide. Subpotent; Beta carotene (Vitamin A)
| Recall number | D-894-2013 |
|---|---|
| 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 | 44118-0775-30, 44118-0800-05, 44118-0800-30 |
| Lot numbers | 10/14, 12080001, 12080002, 12120001, 12120002, 8/14 |
Product
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)
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-894-2013. 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.