F-3356-2017 Class II Terminated
FDA food recall F-3356-2017 was initiated by Duy Drugs Inc. on July 21, 2017 and is designated Class II. Reason for recall: Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements. The recall status is terminated (terminated April 24, 2019). Affected quantity: 411 bottles.
Recall Details
- Product Type
- Food
- Report Date
- August 16, 2017
- Initiation Date
- July 21, 2017
- Termination Date
- April 24, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 411 bottles
Product Description
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Reason for Recall
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Distribution Pattern
Domestic distribution only.
Code Information
Lot No. 1701