FDA recall record

Stayma Consulting Service, LLC Duet DHA 400 ec, containing one 30-count bottle of recall — FDA D-896-2013

Subpotent; Beta carotene (Vitamin A)

Class IIIclassification
D-896-2013official record ID
Aug 28, 2013report date

Recall record at a glance

Official recordD-896-2013
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmStayma Consulting Service, LLC.
Report dateAug 28, 2013
Recall initiation dateJun 28, 2013
QuantityNDC 44118-809-30; 747 and NDC 76331-807-30; 1493
LocationSuwanee, GA, United States

Official product description

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)

Why the product was recalled

Subpotent; Beta carotene (Vitamin A)

Distribution information

Nationwide.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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