FDAFDA · Food and drugs·Recall number D-1182-2018
Levothyroxine and Liothyronine (Thyroid Tablets, USP), 2 grain (120 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-158-04.
Published August 29, 2018 · Recall initiated: August 3, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Westminster Pharmaceuticals LLC
- Distributor
- Nationwide in the USA and Puerto Rico
- Lot
- Lot #: 15817VP-01, 15817VP-02, 15817VP-03, Exp 9/30/2019; 15818001, Exp 3/31/2020.
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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