Cardiovid Plus recall: CGMP Deviations
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Why was Cardiovid Plus recalled?
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
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?
Lot No. 1701
- Product
- Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
- Recalling firm
- Duy Drugs Inc.
- Quantity
- 411 bottles
- Distribution
- Domestic distribution only.
- Recall date
- August 16, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (food)