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 recalls 16 since 2018
Last 12 months 0 reported
Class I 0 0% of total
Ongoing 16 latest 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
Ongoing valsartan and hydrochlorothiazide recalls 16 active
All valsartan and hydrochlorothiazide recalls, newest first 16 total
Reported Class Recall Company Reason Where 23 Jan 2019 Drug CLASS II Valsartan and Hydrochlorothiazide tablets USP 80 mg/12.5 mg recalled Valsartan And Hydrochlorothiazide Aurobindo Pharma USA Nitrosamine Impurity Nationwide 23 Jan 2019 Drug CLASS II Valsartan and Hydrochlorothiazide tablets USP 320mg/12.5 mg recalled Valsartan And Hydrochlorothiazide Aurobindo Pharma USA Nitrosamine Impurity Nationwide 23 Jan 2019 Drug CLASS II Valsartan and Hydrochlorothiazide tablets USP 320 mg/25 mg recalled Valsartan And Hydrochlorothiazide Aurobindo Pharma USA Nitrosamine Impurity Nationwide 23 Jan 2019 Drug CLASS II Valsartan and Hydrochlorothiazide tablets USP 160mg/12.5 mg recalled Valsartan And Hydrochlorothiazide Aurobindo Pharma USA Nitrosamine Impurity Nationwide 23 Jan 2019 Drug CLASS II Valsartan and Hydrochlorothiazide tablets USP 160 mg/25 mg recalled Valsartan And Hydrochlorothiazide Aurobindo Pharma USA Nitrosamine Impurity Nationwide 19 Dec 2018 Drug CLASS II Valsartan and Hydrochlorothiazide Tablets, USP 320/12.5 mg recalled Valsartan And Hydrochlorothiazide Mylan Laboratories Limited, (Nashik FDF) Nitrosamine Impurity Nationwide 19 Dec 2018 Drug CLASS II Valsartan and Hydrochlorothiazide Tablets, USP, 320 mg/25 mg, (a) recalled Valsartan And Hydrochlorothiazide Mylan Pharmaceuticals Nitrosamine Impurity Nationwide 19 Dec 2018 Drug CLASS II Valsartan and Hydrochlorothiazide Tablets, USP 80/12.5 mg recalled Valsartan And Hydrochlorothiazide Mylan Laboratories Limited, (Nashik FDF) Nitrosamine Impurity Nationwide 19 Dec 2018 Drug CLASS II Valsartan and Hydrochlorothiazide Tablets, USP 160/12.5 mg recalled Valsartan And Hydrochlorothiazide Mylan Laboratories Limited, (Nashik FDF) Nitrosamine Impurity Nationwide 19 Dec 2018 Drug CLASS II Valsartan and Hydrochlorothiazide Tablets, USP 160/25 mg recalled Valsartan And Hydrochlorothiazide Mylan Laboratories Limited, (Nashik FDF) Nitrosamine Impurity Nationwide
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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.