Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels

FDA recall notice · announced August 16, 2017 · Duy Drugs

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The product

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.

Notes

Distribution: Domestic distribution only.
Lot/code information: Lot No. 1701
Quantity: 411 bottles
Status: Terminated
Products in this recall event:
- Viva ben Femenine Supplement, Dietary Supplement 30 Softgels (F-3355-2017)
- Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels (F-3356-2017)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.