CLASS II Food recall · Reported 3 Sep 2014 · FDA Enforcement Report

RegeneSlim Appetite Control, Dietary Supplement recalled by Regeneca

Regeneca is recalling RegeneSlim Appetite Control, Dietary Supplement. The recall was initiated on 4 Aug 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes11414RE5516, EX0616R15814, 823230415, EX0616R15813
Quantity recalled154,748 packets

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2403-2014
FDA event ID
68981
Recalling firm
Regeneca, Irvine, CA
Classification
Class II
Status
Terminated
Recall initiated
4 Aug 2014
FDA classified
28 Aug 2014
Reported
3 Sep 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Product category
Weight Loss Supplements

Timeline

4 Aug 2014Recall initiated by company
28 Aug 2014Classified by FDA+24 days
3 Sep 2014Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

RegeneSlim was found to contain DMAA by FDA analysis.

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

RegeneSlim Appetite Control, 2 capsules/ packet, Dietary Supplement

Where it was distributed

Product is sold through multi-level marketing.

Questions about this recall

Why was it recalled?

RegeneSlim was found to contain DMAA by FDA analysis.

Which lots are affected?

11414RE5516, EX0616R15814, 823230415, EX0616R15813

Where was it sold?

Product is sold through multi-level marketing.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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