US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 30, 2018 (8 years ago)

Thyroid powder

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.

What was recalled

Thyroid powder, 4.5 kg foil bag, 5x1 kg foil bags packed in 25 Kg Fiber Drum, Thyroid Powder 25kg/drum, US Pharmacopoeia, Sichuan Friendly Pharmaceutical Co., LTD, Production Address: No. 680, Hongpai Road, Dongxing District, Neijiang City Sichuan, China Tel:+886 832 2240082/2240298, NDC 7807-0170-11

Recalling firm
Alkano Chemicals, Inc
NDC code
7807-0170-11
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0008-2019

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 Ongoing

Thyroid

Reason Subpotent Drug

Specialty Process Labs LLC NDC 81305-100-02 D-0294-2026
Class II · Moderate risk Completed

S.P Labs

Reason Failed Stability Specifications

Specialty Process Labs LLC D-0447-2024
Class II · Moderate risk Completed

S.P.Labs

Reason Failed Stability Specifications

Specialty Process Labs LLC NDC 81305-500-01 D-0446-2024
Class II · Moderate risk Terminated

Armour Thyroid

Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

Cardinal Healthcare D-0168-2024