Balziva recalls
Balziva products have been recalled 2 times, most recently on 2 Jun 2021. The recalling company is usually Teva Pharmaceuticals USA. The most common reason is manufacturing (cgmp) deviations.
Total recalls2since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 2 Jun 2021
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 50%Class III 1 50%
Why balziva is recalled
Companies
Product types
By year
All balziva recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Balziva 28 Day (norethindrone recalled by Cardinal HealthBalziva | Cardinal Health | Manufacturing (CGMP) Deviations | FL, GA, SC |
| Drug | CLASS III | Balziva(TM) (norethindrone and ethinyl estradiol tablets recalledBalziva | Teva Pharmaceuticals USA | Benzene | Nationwide |
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.