Syeda — Class III drug recall D-152-2013
Terminated recall by Sandoz Incorporated, reported 2013-02-13, distributed nationwide. Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could contain the incorrect debossing on one
| Recall number | D-152-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sandoz Incorporated, Broomfield, CO, United States |
| Recall initiated | 2013-01-22 |
| Classified | 2013-02-06 |
| Reported by FDA | 2013-02-13 |
| Terminated | 2013-05-07 |
| Distributed | Nationwide (US) |
| Expiration dates | 2014-02 |
Product
Syeda (drospirenone and ethinyl estradiol), 3 mg/0.03 mg, 3 x 28 tablet blistercards, combination oral contraceptive tablet, Manufactured by Laboratorios Leon Farma S.A., Spain for Sandoz Inc., Princeton, NJ
Reason for recall
Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could contain the incorrect debossing on one side of the tablet U2 instead of U3.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-152-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.