Published recall report · Unapproved ingredientUpdated · 10 yr 4 mo ago
Invisiblu International LLC recall: LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
Current recall status is unverified. FDA does not update drug-enforcement status after publication. Check the latest official information or ask a pharmacist.
What to do
Check the lot number on your pack against this recall and follow the firm's instructions. Do not stop taking a prescribed medicine without talking to a pharmacist or doctor first.
FDA public enforcement report, opens in a new tabWhich products
LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
- Producer
- Invisiblu International LLC
21511166
- Dates on pack
- Lot # 21511166, Exp 11/18
More detail
Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033
In the news
Reporting from news publishers. Follow the official notice for product advice.
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