Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta carotene (Vitamin A)

Date: June 28, 2013
Company: Stayma Consulting Service, LLC.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Stayma Consulting Service, LLC. directly.

Affected Products

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

Quantity: 1) 12,278 and 28476; 2) 23740

Why Was This Recalled?

Subpotent; Beta carotene (Vitamin A)

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Stayma Consulting Service, LLC.

Stayma Consulting Service, LLC. has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report