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FDAFDA · Food and drugs·Recall number D-451-2013

Levothroid (levothyroxine sodium tablets, USP), 200 mcg, RX only, 100 tablets per bottle. Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1327-01

Published May 29, 2013 · Recall initiated: April 1, 2013

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

cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Lloyd Inc. of Iowa
Distributor
The firm distributed the bulk product to Forest Laboratories, Inc, St. Louis, MO who repackaged the product into 100-tablet bottles and distribution was made to 75 customers Nationwide and Puerto Rico.
Lot
Lot #: 1095923, Exp May-13; 1097828, Exp Jul-13.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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