Home / Recalls / Lloyd Inc / D-1393-2012

D-1393-2012 Class II Terminated

Recalled by Lloyd Inc — Shenandoah, IA

Recall Details

Product Type
Drugs
Report Date
July 4, 2012
Initiation Date
February 3, 2012
Termination Date
July 30, 2013
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
19,166 bottles

Product Description

Levothroid (levothyroxine sodium tablets, USP), 50 mcg., packaged in 100-ct. bottles, RX, NDC 0456-1321-01. Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Reason for Recall

Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

Distribution Pattern

Nationwide and PR.

Code Information

Lot 1087589

Other recalls by Lloyd Inc

  • D-1395-2012 Class II — Thyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the (February 24, 2012)
  • D-1394-2012 Class II — Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx o (February 24, 2012)
  • D-1392-2012 Class II — Thyro-Tab 0.050mg., packaged in bulk drums for repackaging. The firm name on th (February 3, 2012)