Why it was recalled
Subpotent; Beta carotene (Vitamin A)
Product description
Duet DHA 430, 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 76331-808-30
Lot numbers, UPCs & expiration codes
NDC 76331-808-30; lot 39736A, exp. 3/14 and lot 41667, exp. 12/14
Where it was sold
Nationwide.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-898-2013
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Jun 28, 2013
- FDA report date
- Aug 28, 2013
- Quantity
- 2985
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Stayma Consulting Service, LLC.
Original FDA data
Every field from FDA enforcement report D-898-2013, exactly as published.
Show all FDA fields
- City
- Suwanee
- State
- GA
- Status
- Terminated
- Country
- United States
- Event ID
- 65663
- Address
- 5400 Laurel Springs Pkwy
- Address (line 2)
- Suite 803
- Code information
- NDC 76331-808-30; lot 39736A, exp. 3/14 and lot 41667, exp. 12/14
- Postal code
- 30024-6056
- Report date
- Aug 28, 2013
- Product type
- Drugs
- Recall number
- D-898-2013
- Classification
- Class III
- Recalling firm
- Stayma Consulting Service, LLC.
- Product quantity
- 2985
- Termination date
- May 27, 2014
- Reason for recall
- Subpotent; Beta carotene (Vitamin A)
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Duet DHA 430, 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 76331-808-30
- Distribution pattern
- Nationwide.
- Recall initiation date
- Jun 28, 2013
- Initial firm notification
- Letter
- Center classification date
- Aug 16, 2013