FDA recall D-103-2013

Lloyd Inc. of Iowa · Class II · drug

Product

Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Reason for recall

Subpotent; 9-month stability interval

Distribution

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

Key facts

Status: Terminated
Initiation date: 2012-07-25
Report date: 2013-01-02
Termination date: 2013-11-14
Voluntary/Mandated: Voluntary: Firm initiated
Location: Shenandoah, IA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-103-2013