# FDA recall D-0014-2019

> **Syntec Pharma Corp** · Class II · drug recall initiated 2018-08-22.

## 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 for recall

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

## Distribution

Al & TX only

## Key facts

- **Recall number:** D-0014-2019
- **Recalling firm:** Syntec Pharma Corp
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-08-22
- **Report date:** 2018-10-17
- **Termination date:** 2024-04-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Farmingdale, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0014-2019

## Citation

> AI Analytics. FDA recall D-0014-2019. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/D-0014-2019. Source: US FDA. Licensed CC0.

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