Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15 mg/0.02 mg and 0.01 mg, 6 Cyclic dispensers X 28 tablets, Rx only Teva Pharmaceuticals, USA, Sellersville, PA. NDC 51285-114-58
Reported: July 23, 2014 Initiated: June 17, 2014 #D-1437-2014
Product Description
Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15 mg/0.02 mg and 0.01 mg, 6 Cyclic dispensers X 28 tablets, Rx only Teva Pharmaceuticals, USA, Sellersville, PA. NDC 51285-114-58
Reason for Recall
Failed Impurities/Degradation Specifications: out of specification impurity test results.
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 984 blister packs
- Distribution
- Nationwide
- Location
- North Wales, PA
Frequently Asked Questions
What product was recalled? ▼
Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15 mg/0.02 mg and 0.01 mg, 6 Cyclic dispensers X 28 tablets, Rx only Teva Pharmaceuticals, USA, Sellersville, PA. NDC 51285-114-58. Recalled by Teva Pharmaceuticals USA. Units affected: 984 blister packs.
Why was this product recalled? ▼
Failed Impurities/Degradation Specifications: out of specification impurity test results.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 23, 2014. Severity: Low. Recall number: D-1437-2014.
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