Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class III · Low risk Terminated Initiated Jun 28, 2013 (13 years ago)

Duet DHA 430 ec

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent; Beta carotene (Vitamin A)

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

What was recalled

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)

Affected NDC 76331-0810-30

Compare with the code on your package — it is the most precise check available.

Recalling firm
Stayma Consulting Service, LLC.
NDC code
76331-810-30
Origin
GA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-899-2013 · FDA notice

Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Stayma Consulting Service, LLC.

All 2013 recalls
Class III · Low risk

Nata Komplete

Subpotent; Beta carotene (Vitamin A)

Terminated Wrong potency / content Stayma Consulting Service, LLC. NDC 76331-909-30 D-900-2013
Class III · Low risk

Duet DHA 430

Subpotent; Beta carotene (Vitamin A)

Terminated Wrong potency / content Stayma Consulting Service, LLC. NDC 76331-808-30 D-898-2013
Class III · Low risk

NataChew

Subpotent; Beta carotene (Vitamin A)

Terminated Wrong potency / content Stayma Consulting Service, LLC. NDC 44118-902-90 D-897-2013

Other wrong potency / content recalls from 2013

All wrong potency / content recalls
Class II · Moderate risk

Clonazepam Tablets

Subpotent Drug: During routine stability testing one tablet was found with tablet weight below specification.

Terminated Wrong potency / content Actavis Elizabeth LLC NDC 0228-3005-11 D-1087-2014