RegeneBlast recalled over manufacturing violations
- Recall date
- March 9, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- VivaCeuticals, Inc. dba Regeneca Worldwide recalls RegeneBlast
- Recall number
- F-1824-2017
- FDA classification
- Class II
- Brand / firm
- VivaCeuticals, Inc. dba Regeneca Worldwide
- Sold / distributed
- US
Why it was recalled
The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
RegeneBlast
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