Avkare Incorporated recalls
Avkare Incorporated has 5 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 12 Sep 2018. The most frequent reason is potency & assay.
Total recalls5since 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 12 Sep 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 5 100%Class III 0 0%
Why avkare incorporated is recalled
Product types
By year
All avkare incorporated recalls, newest first
5 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Valsartan and Hydrochlorothiazide 320 mg recalled by Avkare Incorporated | Avkare Incorporated | Potency & Assay | Nationwide |
| Drug | CLASS II | Valsartan and Hydrochlorothiazide 80 mg/12 recalled | Avkare Incorporated | Potency & Assay | Nationwide |
| Drug | CLASS II | Valsartan and Hydrochlorothiazide 160 mg/12 recalled | Avkare Incorporated | Potency & Assay | Nationwide |
| Drug | CLASS II | Valsartan and Hydrochlorothiazide 160 mg recalled by Avkare Incorporated | Avkare Incorporated | Potency & Assay | Nationwide |
| Drug | CLASS II | Valsartan and Hydrochlorothiazide 320 mg/12 recalled | Avkare Incorporated | 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.