Why it was recalled
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Product description
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Lot numbers, UPCs & expiration codes
Lot No. 1701
Where it was sold
Domestic distribution only.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-3356-2017
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Jul 21, 2017
- FDA report date
- Aug 16, 2017
- Quantity
- 411 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Duy Drugs Inc.
Original FDA data
Every field from FDA enforcement report F-3356-2017, exactly as published.
Show all FDA fields
- City
- Doral
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 77715
- Address
- 1730 NW 79th Ave
- Code information
- Lot No. 1701
- Postal code
- 33126-1111
- Report date
- Aug 16, 2017
- Product type
- Food
- Recall number
- F-3356-2017
- Classification
- Class II
- Recalling firm
- Duy Drugs Inc.
- Product quantity
- 411 bottles
- Termination date
- Apr 24, 2019
- Reason for recall
- Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
- Distribution pattern
- Domestic distribution only.
- Recall initiation date
- Jul 21, 2017
- Initial firm notification
- Center classification date
- Aug 8, 2017