Recalls & Warnings
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Posted September 28, 2017
Seller of Prostate, Reishi Supplements Warned for Manufacturing Violations
On September 11, 2017, the FDA issued a warning letter to Vicare International (USA), Inc., following facility inspections which found a number of the company's products, including VI — DiabeCare, VI — Prosta Care, VI — Sheep Placenta, VI — Vessel Care II, VI — LiverCare, Nu — DiabeCare, Nu — Sheep Placenta, Nu — Prosta Care, Nu — Angio Care, Nu — LiverCare, Vicare Vi-Reishi, NuLife Nu-Reishi, and Vicare Super Cell to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.
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