Next Choice" One Dose Emergency Contraceptive — Class II drug recall D-66360-001
Terminated recall by Watson Laboratories Inc, reported 2013-10-16, distributed nationwide. Failed Tablet/Capsule Specifications: Multiple complaints for push through tablet breakage.
| Recall number | D-66360-001 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Watson Laboratories Inc, Corona, CA, United States |
| Recall initiated | 2013-09-23 |
| Classified | 2013-10-09 |
| Reported by FDA | 2013-10-16 |
| Terminated | 2014-07-25 |
| Distributed | Nationwide (US) |
| Quantity | 1,002,394 tablets |
| Reason classes | device malfunction |
| NDC | 52544-0287-54 |
| Lot numbers | 09/14, 580974AA, 580975AA |
Product
Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet), 1.5 mg, 1 Tablet/Blister Card (NDC 52544-287-54), Manufactured by Watson Laboratories Inc, 132 Business Center Drive, Corona, CA 92880.
Reason for recall
Failed Tablet/Capsule Specifications: Multiple complaints for push through tablet breakage.
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-66360-001. 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.