Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LGD-Xtreme (ligandrol LGD-4033) Recalled by Invisiblu International LLC Due to Marketed Without An Approved NDA/ANDA: Contains an unapproved...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Invisiblu International LLC directly.
Affected Products
LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
Quantity: 3,319 bottles
Why Was This Recalled?
Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Invisiblu International LLC
Invisiblu International LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report