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06-17-2013, 12:21 AM #1
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Recall: Levothroid (levothyroxine sodium tablets, USP) , 50 mcg, RX only
Product Detail
Product Description Levothroid (levothyroxine sodium tablets, USP) , 50 mcg, RX only, 100 tablets per bottle, Manufactured for Forest Pharmaceuticals, Inc, St. Louis, MO by Lloyd Pharmaceutical, Shenandoah, IA, NDC 0456-1321-01
Recall Number D-432-2013
Classification Class II
Code Info Lot #: 1098751, Exp. Mar-13
Product Distributed Qty 4,440 Bottles
Reason For Recall cGMP deviations; After quality review of stability failures in previous lots, there is insufficient data to determine that other lots are not affected.
Event Detail
Event Id 65154
Product Type Drugs
Status Ongoing
Recalling Firm
Lloyd Inc. of Iowa
City Shenandoah
State IA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-04-01
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern
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.
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