Valsartan And Hydrochlorothiazide recalls

Valsartan And Hydrochlorothiazide products have been recalled 16 times, most recently on 23 Jan 2019. The recalling company is usually Prinston Pharmaceutical. The most common reason is nitrosamine impurity.

Total recalls16since 2018
Last 12 months0reported
Class I00% of total
Ongoing16latest 23 Jan 2019

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 16 100%Class III 0 0%

Why valsartan and hydrochlorothiazide is recalled

Product types

By year

Ongoing valsartan and hydrochlorothiazide recalls

16 active

All valsartan and hydrochlorothiazide recalls, newest first

16 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIValsartan and Hydrochlorothiazide tablets USP 80 mg/12.5 mg recalledValsartan And HydrochlorothiazideAurobindo Pharma USANitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide tablets USP 320mg/12.5 mg recalledValsartan And HydrochlorothiazideAurobindo Pharma USANitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide tablets USP 320 mg/25 mg recalledValsartan And HydrochlorothiazideAurobindo Pharma USANitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide tablets USP 160mg/12.5 mg recalledValsartan And HydrochlorothiazideAurobindo Pharma USANitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide tablets USP 160 mg/25 mg recalledValsartan And HydrochlorothiazideAurobindo Pharma USANitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP 320/12.5 mg recalledValsartan And HydrochlorothiazideMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP, 320 mg/25 mg, (a) recalledValsartan And HydrochlorothiazideMylan PharmaceuticalsNitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP 80/12.5 mg recalledValsartan And HydrochlorothiazideMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP 160/12.5 mg recalledValsartan And HydrochlorothiazideMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP 160/25 mg recalledValsartan And HydrochlorothiazideMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide

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.