Thyroid Powder recalled over manufacturing violations
- Recall date
- August 24, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- LGM Pharma LLC recalls Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1
- Recall number
- D-0296-2019
- FDA classification
- Class II
- Brand / firm
- LGM Pharma LLC
- Sold / distributed
- Nationwide in the USA
Why it was recalled
CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1
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