FDA Drug recall D-246-2013
Jolessa (levonorgestrel/ethinyl estradiol) Tablets, 0.15 mg/0.03 mg, 91-count tablets per extended-cycle tablet dispenser packaged in 3 dis…
- FDA Drug
- Class III
- terminated
- Published 2013-04-17
On 2013-04-17 the FDA classified a Class III recall of Jolessa (levonorgestrel/ethinyl estradiol) Tablets, 0.15 mg/0.03 mg, 91-count tablets per extended-cycle tablet dispenser packaged in 3 dis… 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-246-2013 |
| 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
Jolessa (levonorgestrel/ethinyl estradiol) Tablets, 0.15 mg/0.03 mg, 91-count tablets per extended-cycle tablet dispenser packaged in 3 dispensers per carton, Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0555-9123-66.
Reason
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
Identifiers
| ndc | 0555-9123-66 |
|---|---|
| code_info | Lot #: 33803603A, 33803604A, Exp 11/13; 33803996A, and 33803997A, Exp 03/14 |
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-246-2013%22
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