Teva Pharmaceuticals USA, Inc. recalls Portia (levonorgestrel and ethinyl estradiol) Tablets, USP, 0.15 mg/0.03 mg, 28-count tablets (containing 21 pink tablet
Recalled April 17, 2013 · FDA recall D-245-2013 · Teva Pharmaceuticals USA
Hazard
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance. · FDA Class III
Units
17,661 blister cards
Sold at
Nationwide
Description
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Product
Portia (levonorgestrel and ethinyl estradiol) Tablets, USP, 0.15 mg/0.03 mg, 28-count tablets (containing 21 pink tablets followed by 7 white tablets) per blister card packaged in 6 blister cards per carton, Rx only, Barr Laboratories, Inc., Pomona, NY 10970, NDC 0555-9020-58.
Manufacturer(s)
Teva Pharmaceuticals USA, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →