# FDA recall D-1178-2018

> **Westminster Pharmaceuticals LLC** · Class I · drug recall initiated 2018-08-03.

## Product

Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1 grain (60 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-156-04.

## Reason for recall

Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing practices resulted in finished product failing content uniformity specifications which can result in a product having a strength that is more or less than is labeled.

## Distribution

Nationwide in the USA and Puerto Rico

## Key facts

- **Recall number:** D-1178-2018
- **Recalling firm:** Westminster Pharmaceuticals LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-08-03
- **Report date:** 2018-08-29
- **Termination date:** 2020-06-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Olive Branch, MS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1178-2018

## Citation

> AI Analytics. FDA recall D-1178-2018. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-1178-2018. Source: US FDA. Licensed CC0.

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