FDA Drug recall D-0014-2019
THYROID POWDER USP (Levothyroxine labeled range of 34.2-41.8mcg/grain
- FDA Drug
- Class II
- terminated
- Published 2018-10-17
On 2018-10-17 the FDA classified a Class II recall of THYROID POWDER USP (Levothyroxine labeled range of 34.2-41.8mcg/grain by Syntec Pharma, citing CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0014-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-08-22 |
| Published | 2018-10-17 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Syntec Pharma |
| Distribution | TX |
Product
THYROID POWDER USP (Levothyroxine labeled range of 34.2-41.8mcg/grain; Liothyroine (correct spelling Liothyronine): labeled range of 8.1-9.9mcg/grain) active pharmaceutical ingredient; 25 KG bag, Rx Compounding only, Manu By: Sichuan Friendly Pharmaceutical Co., Ltd., No. 680 Hongpai Road, Neijiang, sichuan 641000, china; Distributed: Syntec Pharma Corp., 96 Gazza Blvd., Farmingdale NY 11735, CAS No. 50809-32-0
Reason
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Identifiers
| code_info | All lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0014-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.