Class II
Terminated
ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY
This recall has been terminated (originally issued June 4, 2014).
- Company
- Teva Pharmaceuticals Usa
- Recall Initiated
- March 21, 2014
- Posted
- June 4, 2014
- Recall Number
- D-1354-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 47890
- Firm Location
- Horsham, PA, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Non-sterility: due to a failed sterility test
Distribution
NY and 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
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