US Drug Recall Register
Class I · High risk Terminated Initiated Dec 9, 2016 (10 years ago)

SLIMFIT X capsules, packaged in a 60-cont bottle

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

Why it was recalled

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

What was recalled

SLIMFIT X capsules, packaged in a 60-cont bottle

Recalling firm
Jersey Shore Supplements, LLC
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0473-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.