Lloyd Inc. of Iowa recalls

Lloyd Inc. of Iowa has 36 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 29 May 2013. The most frequent reason is potency & assay.

Total recalls36since 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 36 100%Class III 0 0%

Why lloyd inc. of iowa is recalled

Product types

By year

All lloyd inc. of iowa recalls, newest first

36 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILloyd Thyro-Tab 0.200 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 175 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILloyd Thyro-Tab 0.175 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILloyd Thyro-Tab 0.137 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP) , 125 mcg recalledLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILloyd Thyro-Tab 0.100 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILloyd Thyro-Tab 0.125 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILloyd Thyro-Tab 0.088 mg recalled by Lloyd Inc. of IowaLloyd 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 IILloyd Thyro-Tab 0.112 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILloyd Thyro-Tab 0.075 mg recalled by Lloyd Inc. of IowaLloyd 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 IILloyd Thyro-Tab 0.150 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IILloyd Thyro-Tab 0.050 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IIThyro-Tab 0.050 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaPotency & AssayNationwide
DrugCLASS IIThyro-Tab 0.075 mg recalled by Lloyd Inc. of IowaLloyd 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 IIThyro-Tab 0.088 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIThyro-Tab 0.300 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIThyro-Tab 0.125 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 50 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIThyro-Tab 0.112 mg recalled by Lloyd Inc. of IowaLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILevothroid (levothyroxine sodium tablets, USP), 300 mcg recalledLloyd Inc. of IowaManufacturing (CGMP) DeviationsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.