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.
Reported: April 17, 2013 Initiated: March 12, 2013 #D-245-2013
Product Description
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.
Reason for Recall
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Details
- Recalling Firm
- Teva Pharmaceuticals USA, Inc.
- Units Affected
- 17,661 blister cards
- Distribution
- Nationwide
- Location
- Sellersville, PA
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Teva Pharmaceuticals USA, Inc.. Units affected: 17,661 blister cards.
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 17, 2013. Severity: Low. Recall number: D-245-2013.
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