US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Mar 31, 2016 (10 years ago)

LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033

What was recalled

LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL

Recalling firm
Invisiblu International LLC
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0910-2016

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.