FDA Drug recall D-66360-001
Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet), 1.5 mg, 1 Tablet/Blister Card (NDC 52544-287-54), Manufactured by Wa…
- FDA Drug
- Class II
- terminated
- Published 2013-10-16
On 2013-10-16 the FDA classified a Class II recall of Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet), 1.5 mg, 1 Tablet/Blister Card (NDC 52544-287-54), Manufactured by Wa… by Watson Laboratories, citing failed Tablet/Capsule Specifications: Multiple complaints for push through tablet breakage.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-66360-001 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-23 |
| Published | 2013-10-16 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Watson Laboratories |
| Distribution | US |
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
Failed Tablet/Capsule Specifications: Multiple complaints for push through tablet breakage.
Identifiers
| code_info | Lot#: 580974AA and 580975AA. Exp: 09/14 |
|---|
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-66360-001%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.