Losartan Potassium recalls

Losartan Potassium products have been recalled 20 times, most recently on 12 Jul 2023. The recalling company is usually Macleods Pharma Usa. The most common reason is potency & assay.

Total recalls20since 2019
Last 12 months0reported
Class I00% of total
Ongoing3latest 12 Jul 2023

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 losartan potassium is recalled

Product types

By year

Ongoing losartan potassium recalls

3 active

All losartan potassium recalls, newest first

20 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILosartan Potassium Tablets, USP, 25 mg recalled by Strides PharmaLosartan PotassiumStrides PharmaForeign MaterialNationwide
DrugCLASS IILosartan Potassium Tablets, USP 25 mg recalled by PD-Rx PharmaceuticalsLosartan PotassiumPD-Rx PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets, USP 100 mg recalled by PD-Rx PharmaceuticalsLosartan PotassiumPD-Rx PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets, USP 50 mg recalled by PD-Rx PharmaceuticalsLosartan PotassiumPD-Rx PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets, USP 25 mg recalled by Strides PharmaLosartan PotassiumStrides PharmaPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets, USP, 100 mg recalled by Strides PharmaLosartan PotassiumStrides PharmaPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets, USP, 50 mg recalled by Strides PharmaLosartan PotassiumStrides PharmaPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets USP, 25 mg, a) bottles recalledLosartan PotassiumLupin PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets USP, 50 mg, a) bottles recalledLosartan PotassiumLupin PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILosartan Potassium Tablets, USP, 100 mg, a) bottles recalledLosartan PotassiumMacleods Pharma UsaPotency & AssayNationwide

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.