Teva Pharmaceuticals USA recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, (CII), 1
Recalled August 12, 2015 · FDA recall D-1283-2015 · Teva Pharmaceuticals USA
Hazard
Failed Impurities/Degradation Specifications: out of specification for unknown impurity · FDA Class II
Units
19,504 bottles
Sold at
Nationwide
Description
Failed Impurities/Degradation Specifications: out of specification for unknown impurity
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, (CII), 10 mg (Mixed Salts of a Single Entity Amphetamine Product), 100 count bottles, manufactured at Barr Laboratories, Inc. Forest, VA for Teva Pharmaceuticals USA, Sellersville, PA --- NDC 0555-0972-02
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →