drugs Class II Updated 2014-06-04

Teva Pharmaceuticals USA recalls ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg

Recalled Product

ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY

Hazard / Issue

Non-sterility: due to a failed sterility test

Issued by

FDA

Affected States: NY, KY
Lot/Code Info: 508004, exp. 4/2015, NDC 51285-204-01, Single Unit 508004, exp. 4/2015, NDC 51285-204-02, Carton of 5 Units
View official government recall

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