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 month

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why dextroamphetamine sulfate is recalled

Product types

By year

All dextroamphetamine sulfate recalls, newest first

3 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIDextroamphetamine Sulfate Extended-Release Capsules, 10 mg recalledDextroamphetamine SulfateActavisPotency & AssayNationwide
DrugCLASS IIDextroamphetamine Sulfate Extended-Release Capsules, 15 mg recalledDextroamphetamine SulfateActavis ElizabethPotency & AssayNationwide
DrugCLASS IIDextroamphetamine Sulfate Tablets, USP, 10 mg recalledDextroamphetamine SulfateTeva Pharmaceuticals UPotency & AssayNationwide

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.