Duy Drugs Recalls Cardiovid Plus Dietary Supplement for CGMP Violations
Duy Drugs Inc. is recalling 411 bottles of Cardiovid Plus dietary supplements because they failed to meet FDA current good manufacturing practice requirements.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a moderate severity score under the rubric for manufacturing violations without reported injuries or specific high-risk pathogens.
Plain-English summary
Duy Drugs Inc. is recalling 411 bottles of Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels. The recall is limited to Lot No. 1701. The product was distributed domestically.
The recall was initiated because the product failed to meet 21 CFR Part 111, which outlines current good manufacturing practices (CGMPs) for dietary supplements. Specifically, the failure involved assuring the identity, purity, and composition of the dietary supplements.
Consumers who have this product should stop using it and contact Duy Drugs Inc. for further instructions or a refund.
The recalled product
- Product
- Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
- Manufacturer
- Duy Drugs Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 411
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot No. 1701
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 2 recalled by Duy Drugs Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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