Teva Pharmaceuticals USA recalls ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of
Recalled June 4, 2014 · FDA recall D-1354-2014 · Teva Pharmaceuticals USA
Hazard
Non-sterility: due to a failed sterility test · FDA Class II
Units
47890
Sold at
NY and KY
Description
Non-sterility: due to a failed sterility test
Product
ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →