Apri recalls
Apri products have been recalled 1 time, most recently on 23 Jul 2014. The recalling company is usually Teva Pharmaceuticals U. The most common reason is potency & assay.
Total recalls1since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 23 Jul 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 1 100%
Why apri is recalled
Companies
Product types
By year
All apri recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Apri (desogestrel and ethinyl estradiol tablets USP) recalledApri | Teva Pharmaceuticals U | Potency & Assay | 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.