RegeneSlim
Recalled by VivaCeuticals, INC. DBA Regeneca Worldwide on Mar 9, 2017
Recall Summary
VivaCeuticals, INC. DBA Regeneca Worldwide recalled RegeneSlim in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Mar 9, 2017.
The FDA-published reason for this recall is: "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."
Distribution was limited; the FDA record lists "US." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in Irvine, CA. The recall covers 4000 units of product. The FDA has Terminated this recall (first reported Apr 12, 2017), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.
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.
Product Description
RegeneSlim
Distribution
US
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Terms Explained
- Class II Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.