FDAFDA · Food and drugs·Recall number D-245-2013
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.
Published April 17, 2013 · Recall initiated: March 12, 2013
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 Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PORTIA
- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 33801951A, and 33802189A, Exp 03/13
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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