Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen), 0.1 mg/0.025 mg; 0.125 mg/0.025 mg; 0.15 mg/0.025 mg, 3 Dispensers x 28 Tablets, Barr Laboratories, Inc., Pomona, NY NDC 0555-9051-67
Reported: July 23, 2014 Initiated: June 17, 2014 #D-1439-2014
Product Description
Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen), 0.1 mg/0.025 mg; 0.125 mg/0.025 mg; 0.15 mg/0.025 mg, 3 Dispensers x 28 Tablets, Barr Laboratories, Inc., Pomona, NY NDC 0555-9051-67
Reason for Recall
Failed Impurities/Degradation Specifications: out of specification impurity test results.
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 5265 blister packs
- Distribution
- Nationwide
- Location
- North Wales, PA
Frequently Asked Questions
What product was recalled? ▼
Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen), 0.1 mg/0.025 mg; 0.125 mg/0.025 mg; 0.15 mg/0.025 mg, 3 Dispensers x 28 Tablets, Barr Laboratories, Inc., Pomona, NY NDC 0555-9051-67. Recalled by Teva Pharmaceuticals USA. Units affected: 5265 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-1439-2014.
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