Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Terminated Initiated Oct 28, 2016 (10 years ago)

Skinny Bee Diet capsules

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Marketed without an approved NDA/ANDA: presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and phenolphthalein.

Cause type: Chemical / undeclared

A chemical that should not be there - benzene, methanol, lead - or an undeclared prescription drug hidden in a supplement. The label gives no warning: you may be taking a toxic solvent, a heavy metal, or a drug such as sildenafil that interacts with your other medicines. All chemical / undeclared recalls.

What was recalled

Skinny Bee Diet capsules, 500 mg, packaged in a 60-count bottle

Recalling firm
Love My Tru Body
Origin
GA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0223-2017 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other chemical / undeclared recalls from 2016

All chemical / undeclared recalls
Class I · High risk

SLIMFIT X capsules

Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine.

Terminated Chemical / undeclared Jersey Shore Supplements, LLC D-0473-2017
Class I · High risk

MegaJex Herbal Supplement

Marketed without an Approved NDA/ANDA; product contains sildenafil and tadalafil which are active pharmaceutical ingredients in FDA approved drugs used to treat erectile dysfunction (ED)

Terminated Chemical / undeclared MS Bionic D-0472-2017
Class I · High risk

Ultimate Body Tox PRO capsules

Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine. The presence of sibutramine, a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons, in this tainted product renders it an unapproved drug for which safety and efficacy have not been established and therefore subject to recall.

Terminated Chemical / undeclared Ultimate Body Tox D-0210-2017