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Recall Observatory FDA recall evidence

Drug product

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

D-101-2013

July 25, 2012

Class II

Product summary

Firm
Lloyd Inc. of Iowa
Event
Event 62664
Status
Terminated
Classification
Class II
Quantity
37,441/100-tablet bottles
Official record key
drug-enforcement:D-101-2013

Official wording

Reason: Subpotent; 9-month stability interval

Code information: Lot 1093992 and 1094095, exp. date 9/2012

Distribution pattern: Distribution was nationwide and to Puerto Rico. There was no foreign, military, or government distribution.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Subpotent