FDAClass IIIAugust 28, 2013

Duet DHA 430 recall: Subpotent

Duet DHA 430, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules…

Why was Duet DHA 430 recalled?

Subpotent; Beta carotene (Vitamin A)

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

NDC 76331-808-30; lot 39736A, exp. 3/14 and lot 41667, exp. 12/14

Product
Duet DHA 430, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules…
Recalling firm
Stayma Consulting Service, LLC.
Quantity
2985
Distribution
Nationwide.
Recall date
August 28, 2013
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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