Thyroid Powder — Class II drug recall D-0296-2019
Terminated recall by LGM Pharma LLC, reported 2018-12-19, distributed nationwide. CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyroni
| Recall number | D-0296-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LGM Pharma LLC, Erlanger, KY, United States |
| Recall initiated | 2018-08-24 |
| Classified | 2018-12-12 |
| Reported by FDA | 2018-12-19 |
| Terminated | 2023-09-11 |
| Distributed | Nationwide (US) |
| Quantity | 1,307 kilograms |
| Reason classes | cgmp |
| Lot numbers | 161101, 161201, 170301, 170501, 170701 |
| Expiration dates | 2016-11-02, 2018-11-20, 2019-02-20, 2019-04-20, 2019-06-20 |
Product
Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1
Reason for recall
CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0296-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.