RegeneSlim

FDA recall notice · announced April 12, 2017 · Vivaceuticals, Inc. Dba Regeneca Worldwide

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

The product

RegeneSlim

Reason for recall

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.

Notes

Distribution: US
Lot/code information: Lot AAMXG
Quantity: 4000 units
Status: Terminated
Products in this recall event:
- RegeneBlend (F-1822-2017)
- RegeneArouse (F-1821-2017)
- RegeneBlast (F-1824-2017)
- RegeneFit (F-1825-2017)
- RegeneBoost (F-1823-2017)
- RegenErect (F-1820-2017)
- RegeneSlim (F-1819-2017)

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