FDA recall record

Sichuan Friendly Pharmaceutical Co Thyroid Powder 25kg/drum, US Pharmacopoeia, Sichuan recall — FDA D-0006-2019

CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.

Class IIclassification
D-0006-2019official record ID
Oct 10, 2018report date

Recall record at a glance

Official recordD-0006-2019
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSichuan Friendly Pharmaceutical Co., Ltd.
Report dateOct 10, 2018
Recall initiation dateAug 21, 2018
Quantity2662 kg
LocationNeijiang, China

Official product description

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

Why the product was recalled

CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.

Distribution information

Distributed nationwide and China

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.