ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY
Reported: June 4, 2014 Initiated: March 21, 2014 #D-1354-2014
Product Description
ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY
Reason for Recall
Non-sterility: due to a failed sterility test
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 47890
- Distribution
- NY and KY
- Location
- Horsham, PA
Frequently Asked Questions
What product was recalled? ▼
ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY. Recalled by Teva Pharmaceuticals USA. Units affected: 47890.
Why was this product recalled? ▼
Non-sterility: due to a failed sterility test
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 4, 2014. Severity: Moderate. Recall number: D-1354-2014.
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