Class II · Moderate risk Ongoing
Thyroid
Reason Subpotent Drug
Thyroid Powder
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
What was recalled
Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1
- Recalling firm
- LGM Pharma LLC
- Origin
- KY, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0296-2019
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Thyroid recalls
See all
Class II · Moderate risk Completed
S.P Labs
Reason Failed Stability Specifications
Class II · Moderate risk Completed
S.P.Labs
Reason Failed Stability Specifications
Class II · Moderate risk Terminated
Levothyroxine 25mcg in Ns 1.25ml Syringe
Reason Lack of sterility assurance
Class II · Moderate risk Terminated
Armour Thyroid
Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
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