FDA recall D-1394-2012

Lloyd Inc · 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, Iowa 51601

Reason for recall

Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

Distribution

Nationwide

Key facts

Status: Terminated
Initiation date: 2012-02-24
Report date: 2012-07-04
Termination date: 2013-07-30
Voluntary/Mandated: Voluntary: Firm initiated
Location: Shenandoah, IA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1394-2012