RegeneSlim Appetite Control, 2 capsules/ packet, Dietary Supplement
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2403-2014.
RegeneSlim was found to contain DMAA by FDA analysis.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2403-2014.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Regeneca, Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2403-2014.
Regeneca, Inc
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Regeneca, Inc Recall FAQ
Regeneca, Inc is the subject of a supplements safety report: RegeneSlim Appetite Control, 2 capsules/ packet, Dietary Supplement. The notice was published on August 4, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 154,748 units are potentially affected.