# FDA recall D-896-2013

> **Stayma Consulting Service, LLC.** · Class III · drug recall initiated 2013-06-28.

## Product

Duet DHA 400 ec, 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 44118-809-30) and Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-809-30)

## Reason for recall

Subpotent; Beta carotene (Vitamin A)

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-896-2013
- **Recalling firm:** Stayma Consulting Service, LLC.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-06-28
- **Report date:** 2013-08-28
- **Termination date:** 2014-05-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Suwanee, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-896-2013

## Citation

> AI Analytics. FDA recall D-896-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-896-2013. Source: US FDA. Licensed CC0.

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