RecallDepth
Class II Ongoing

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

This recall is currently active, issued June 8, 2016. It was issued by Invisiblu International Llc.

Company
Invisiblu International Llc
Recall Initiated
March 31, 2016
Posted
June 8, 2016
Recall Number
D-0910-2016
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
3,319 bottles
Firm Location
Fort Lauderdale, FL, United States
Official Source
View on FDA website ↗

Reason for Recall

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

Distribution

Nationwide and Brazil.

Lot / Code Info

Lot # 21511166, Exp 11/18

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