Duet DHA 400 recall: Subpotent
Duet DHA 400, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Rx only…
Why was Duet DHA 400 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 44118-807-30 Lots 40614, exp. 9/14 and 40614A, exp. 9/14 NDC 76331-807-30 lot 39736A, exp. 3/2014, and lot 41667, exp. 12/2014
- Product
- Duet DHA 400, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Rx only…
- Recalling firm
- Stayma Consulting Service, LLC.
- Quantity
- 1,460 and 2,990
- Distribution
- Nationwide.
- Recall date
- August 28, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)