Dextroamphetamine Sulfate recalls
Dextroamphetamine Sulfate products have been recalled 3 times, most recently on 3 Aug 2016. The recalling company is usually Actavis Elizabeth. The most common reason is potency & assay.
Total recalls3since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 3 Aug 2016
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why dextroamphetamine sulfate is recalled
Companies
Product types
By year
All dextroamphetamine sulfate recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Dextroamphetamine Sulfate Extended-Release Capsules, 10 mg recalledDextroamphetamine Sulfate | Actavis | Potency & Assay | Nationwide |
| Drug | CLASS II | Dextroamphetamine Sulfate Extended-Release Capsules, 15 mg recalledDextroamphetamine Sulfate | Actavis Elizabeth | Potency & Assay | Nationwide |
| Drug | CLASS II | Dextroamphetamine Sulfate Tablets, USP, 10 mg recalledDextroamphetamine Sulfate | 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.