Reported Jun 4, 2014 · Terminated
ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary…
Teva Pharmaceuticals USA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Teva Pharmaceuticals USA · 425 Privet Rd · Horsham, PA · 19044-1220
Is this the product you have?
- ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY
- Lot codes and dates
508004exp. 4/2015NDC 51285-204-01Single Unit 508004exp. 4/2015NDC 51285-204-02Carton of 5 Units
- Amount recalled
- 47890
Where it was sold
Why it was recalled
Non-sterility: due to a failed sterility test
This product could cause temporary or reversible health problems — stop using it.
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