FDA Drug recall 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 whi…
- FDA Drug
- Class III
- terminated
- Published 2013-04-17
On 2013-04-17 the FDA classified a Class III recall of Portia (levonorgestrel and ethinyl estradiol) Tablets, USP, 0.15 mg/0.03 mg, 28-count tablets (containing 21 pink tablets followed by 7 whi… by Teva Pharmaceuticals Usa, citing failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-245-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-03-12 |
| Published | 2013-04-17 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Teva Pharmaceuticals Usa |
| Distribution | US |
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.
Reason
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Identifiers
| ndc | 0555-9020-79 |
|---|---|
| ndc | 0555-9020-58 |
| code_info | Lot #: 33801951A, and 33802189A, Exp 03/13 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-245-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.