Mylan Laboratories Limited, (Nashik FDF) recalls

Mylan Laboratories Limited, (Nashik FDF) has 13 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 19 Dec 2018. 13 are still ongoing. The most frequent reason is nitrosamine impurity.

Total recalls13since 2018
Last 12 months0reported
Class I00% of total
Ongoing13latest 19 Dec 2018

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 13 100%Class III 0 0%

Why mylan laboratories limited, (nashik fdf) is recalled

Product types

By year

Ongoing mylan laboratories limited, (nashik fdf) recalls

13 active

All mylan laboratories limited, (nashik fdf) recalls, newest first

13 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIAmlodipine and Valsartan Tablets, USP 10/320 mg recalledAmlodipine And ValsartanMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan Tablets, USP 40 mg recalled by Mylan Laboratories LimitedValsartanMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP 320/12.5 mg recalledValsartan And HydrochlorothiazideMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIAmlodipine and Valsartan Tablets, USP 5/320 mg recalledAmlodipine And ValsartanMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIAmlodipine and Valsartan Tablets, USP 5/160 mg recalledAmlodipine And ValsartanMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP 80/12.5 mg recalledValsartan And HydrochlorothiazideMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan Tablets, USP 160 mg recalled by Mylan Laboratories LimitedValsartanMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIAmlodipine and Valsartan Tablets, USP 10/160 mg recalledAmlodipine And ValsartanMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan Tablets, USP 80 mg recalled by Mylan Laboratories LimitedValsartanMylan Laboratories Limited, (Nashik FDF)Nitrosamine ImpurityNationwide
DrugCLASS IIValsartan Tablets, USP 320 mg recalled by Mylan Laboratories LimitedValsartanMylan 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
DrugCLASS IIValsartan and Hydrochlorothiazide Tablets, USP 320/25 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.