Teva Pharmaceuticals USA recalls Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15 mg/0.02 mg and 0.01 mg, 6 Cyclic dispensers
Recalled July 23, 2014 · FDA recall D-1438-2014 · Teva Pharmaceuticals USA
Hazard
Failed Impurities/Degradation Specifications: out of specification impurity test results. · FDA Class III
Units
1125 blister packs
Sold at
Nationwide
Description
Failed Impurities/Degradation Specifications: out of specification impurity test results.
Product
Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15 mg/0.02 mg and 0.01 mg, 6 Cyclic dispensers X 28 tablets, Rx only, Teva Pharmaceuticals, Sellersville, PA NDC 0555-9050-58
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →