FDAFDA · Food and drugs·Recall number D-1439-2014
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
Published July 23, 2014 · Recall initiated: June 17, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications: out of specification impurity test results.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- VELIVET
- Manufacturer
- Teva Pharmaceuticals USA
- Distributor
- Nationwide
- Lot
- Lot 33805449A, Exp. 12/14
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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