Invisiblu International LLC recalls LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
Recalled June 8, 2016 · FDA recall D-0910-2016 · Invisiblu International
Hazard
Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033 · FDA Class II
Units
3,319 bottles
Sold at
Nationwide and Brazil.
Description
Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033
Product
LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
Manufacturer(s)
Invisiblu International LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →