Levothroid (levothyroxine recalls

The FDA has published 20 recalls involving Levothroid (levothyroxine since 2012. The latest was reported on 29 May 2013. Most were for potency & assay. Lloyd Inc. of Iowa has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls20since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 29 May 2013

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 20 100%Class III 0 0%

Why levothroid (levothyroxine is recalled

Companies

By year

All levothroid (levothyroxine recalls, newest first

20 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 175 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP) , 125 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP) , 75 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 100 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 200 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 88 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP) , 50 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 150 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 112 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 137 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 50 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 75 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 50 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 300 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 88 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP),125 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 137 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 112 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 50 mcg recalled by LloydLloydPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 75 mcg recalled by LloydLloydPotency & AssayNationwide

Should you stop taking Levothroid (levothyroxine?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.