Reported Jun 8, 2016 · Ongoing
LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
Invisiblu International LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Invisiblu International LLC · 620 SE 13th St · Fort Lauderdale, FL · 33316-2023
Is this the product you have?
- LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
- Lot codes and dates
Lot # 21511166Exp 11/18
- Amount recalled
- 3,319 bottles
Where it was sold
- Nationwide
Why it was recalled
Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033
This product could cause temporary or reversible health problems — stop using it.
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